A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672633



Internal ID9938738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176561667..176567487hg38UCSC Ensembl
Outerchr5:176561630..176567537hg38UCSC Ensembl
Innerchr5:175988668..175994488hg19UCSC Ensembl
Outerchr5:175988631..175994538hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg385908
hg195908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1057e199
Supporting Variantsessv6069203
SamplesHG00651
Known GenesCDHR2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672633
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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