A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032667



Internal ID19121889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2691667..2788242hg38UCSC Ensembl
Innerchr9:2691667..2788242hg19UCSC Ensembl
Innerchr9:2681667..2778242hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3896576
hg1996576
hg1896576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692365
Samples
Known GenesKCNV2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032667
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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