A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670879



Internal ID9590298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35169413..35175119hg38UCSC Ensembl
Outerchr19:35169042..35175489hg38UCSC Ensembl
Innerchr19:35660316..35666022hg19UCSC Ensembl
Outerchr19:35659945..35666392hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386448
hg196448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv636e199
Supporting Variantsessv5453620, essv6379824, essv5786461, essv5434268, essv5741866, essv5468737, essv5752978, essv6393593, essv6032728, essv5754946, essv5501705, essv6007617, essv6018506, essv6419055, essv6463303, essv6203455, essv6102446, essv5547848, essv6374967, essv5704800, essv6311673, essv5513561, essv5663909, essv5995718, essv6292128, essv5953428, essv6497475, essv5577666, essv6106153, essv6024757, essv5690358, essv6521627, essv6544398, essv6290791, essv5970038
SamplesHG00626, HG00650, HG00608, HG00559, HG00524, HG00693, HG00663, HG00589, HG00501, HG00702, HG00448, HG00634, HG00610, HG00537, HG00512, HG00683, HG00705, HG00427, HG00530, HG00629, HG00436, HG00708, HG00692, HG00404, HG00479, HG00613, HG00525, HG00704, HG00473, HG00620, HG00672, HG00656, HG00698, HG00472, HG00593
Known GenesFXYD5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670879
Frequency
Sample Size1151
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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