A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615215



Internal ID6655414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139497696..139531755hg38UCSC Ensembl
Innerchr7:139497846..139531605hg38UCSC Ensembl
Outerchr7:139497546..139531905hg38UCSC Ensembl
chr7:139182442..139216501hg19UCSC Ensembl
Innerchr7:139182592..139216351hg19UCSC Ensembl
Outerchr7:139182292..139216651hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3834060
hg1934060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12982068, essv12982069, essv12982067
SamplesHG02890, HG03382, HG03410
Known GenesCLEC2L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615215
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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