A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526410



Internal ID8420685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:151017725..151078219hg38UCSC Ensembl
Innerchr7:150714812..150775306hg19UCSC Ensembl
Innerchr7:150345745..150406239hg18UCSC Ensembl
Innerchr7:150152460..150212954hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3860495
hg1960495
hg1860495
hg1760495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702710
Samples
Known GenesABCB8, ASIC3, ATG9B, CDK5, FASTK, SLC4A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526410
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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