A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700012



Internal ID15436664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85543631..85845149hg38UCSC Ensembl
Innerchr9:88158546..88460064hg19UCSC Ensembl
Innerchr9:87348366..87649884hg18UCSC Ensembl
Innerchr9:85388100..85689618hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38301519
hg19301519
hg18301519
hg17301519
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524134
Supporting Variants
Samples
Known GenesAGTPBP1, LOC389765
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700012
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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