A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3694904



Internal ID18646499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40915718..41113170hg38UCSC Ensembl
Innerchr9:68828665..69186399hg19UCSC Ensembl
Innerchr9:68218485..68476219hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38197453
hg19357735
hg18257735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019779
Supporting Variants
Samples
Known GenesLOC440896, PGM5P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3694904
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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