A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638375



Internal ID7025161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29882924..29884617hg38UCSC Ensembl
Innerchr16:29882960..29884581hg38UCSC Ensembl
Outerchr16:29882888..29884653hg38UCSC Ensembl
chr16:29894245..29895938hg19UCSC Ensembl
Innerchr16:29894281..29895902hg19UCSC Ensembl
Outerchr16:29894209..29895974hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381694
hg191694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15441729, essv15441731, essv15441730, essv15441727, essv15441728, essv15441726
SamplesHG02026, HG02061, HG01849, HG01858, HG02049, NA19072
Known GenesSEZ6L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638375
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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