A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658400



Internal ID15048366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124290188..124357163hg38UCSC Ensembl
Innerchr9:127052467..127119442hg19UCSC Ensembl
Innerchr9:126092288..126159263hg18UCSC Ensembl
Innerchr9:124132021..124198996hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3866976
hg1966976
hg1866976
hg1766976
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519767
Supporting Variants
Samples
Known GenesLOC100129034, NEK6, PSMB7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658400
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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