A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515561



Internal ID15443172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155119771..155123141hg38UCSC Ensembl
Innerchr7:154911481..154914851hg19UCSC Ensembl
Innerchr7:154542414..154545784hg18UCSC Ensembl
Innerchr7:154349129..154352499hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg383371
hg193371
hg183371
hg173371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692525, nssv663908, nssv664793, nssv659951, nssv661727, nssv693021
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515561
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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