A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658314



Internal ID15048280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485135..69497351hg38UCSC Ensembl
Innerchr9:72100051..72112267hg19UCSC Ensembl
Innerchr9:71289871..71302087hg18UCSC Ensembl
Innerchr9:69329605..69341821hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3812217
hg1912217
hg1812217
hg1712217
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515519
Supporting Variants
Samples
Known GenesAPBA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658314
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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