A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519125



Internal ID15099732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85075131..85166394hg38UCSC Ensembl
Innerchr7:84704447..84795710hg19UCSC Ensembl
Innerchr7:84542383..84633646hg18UCSC Ensembl
Innerchr7:84349098..84440361hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3891264
hg1991264
hg1891264
hg1791264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696602
Samples
Known GenesSEMA3D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519125
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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