A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527116



Internal ID15454409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138701844..138703034hg38UCSC Ensembl
Innerchr7:138386589..138387779hg19UCSC Ensembl
Innerchr7:138037129..138038319hg18UCSC Ensembl
Innerchr7:137843844..137845034hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381191
hg191191
hg181191
hg171191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703498
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527116
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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