A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613634



Internal ID6653843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71607775..71611041hg38UCSC Ensembl
Innerchr7:71607793..71611024hg38UCSC Ensembl
Outerchr7:71607758..71611059hg38UCSC Ensembl
chr7:71072760..71076026hg19UCSC Ensembl
Innerchr7:71072778..71076009hg19UCSC Ensembl
Outerchr7:71072743..71076044hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg383267
hg193267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12829736
SamplesHG01935
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613634
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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