A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613805



Internal ID6654013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77684823..77692571hg38UCSC Ensembl
Innerchr7:77684833..77692561hg38UCSC Ensembl
Outerchr7:77684813..77692581hg38UCSC Ensembl
chr7:77314140..77321888hg19UCSC Ensembl
Innerchr7:77314150..77321878hg19UCSC Ensembl
Outerchr7:77314130..77321898hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg387749
hg197749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12857905
SamplesHG00269
Known GenesRSBN1L-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613805
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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