A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034003



Internal ID18776537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6663786..6745551hg38UCSC Ensembl
Innerchr9:6663786..6745551hg19UCSC Ensembl
Innerchr9:6653786..6735551hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3881766
hg1981766
hg1881766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7390n100
Supporting Variantsnssv3689091
Samples
Known GenesKDM4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034003
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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