A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613741



Internal ID7000636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75825701..75827033hg38UCSC Ensembl
Innerchr7:75825722..75827012hg38UCSC Ensembl
Outerchr7:75825680..75827054hg38UCSC Ensembl
chr7:75455019..75456351hg19UCSC Ensembl
Innerchr7:75455040..75456330hg19UCSC Ensembl
Outerchr7:75454998..75456372hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381333
hg191333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848229
SamplesNA18553
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613741
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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