A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524928



Internal ID8419203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:151034611..151069712hg38UCSC Ensembl
Innerchr7:150731698..150766799hg19UCSC Ensembl
Innerchr7:150362631..150397732hg18UCSC Ensembl
Innerchr7:150169346..150204447hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3835102
hg1935102
hg1835102
hg1735102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700941
Samples
Known GenesABCB8, ASIC3, CDK5, SLC4A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524928
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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