A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607956



Internal ID6994887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4733595..4736055hg38UCSC Ensembl
Innerchr6:4733595..4736055hg38UCSC Ensembl
Outerchr6:4733322..4736355hg38UCSC Ensembl
chr6:4733829..4736289hg19UCSC Ensembl
Innerchr6:4733829..4736289hg19UCSC Ensembl
Outerchr6:4733556..4736589hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382461
hg192461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12179527, essv12179524, essv12179528, essv12179526, essv12179523, essv12179525
SamplesHG00851, HG02397, HG00701, HG00473, HG00478, HG02392
Known GenesCDYL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607956
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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