A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025847



Internal ID19115064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6701133..6725007hg38UCSC Ensembl
Innerchr9:6701133..6725007hg19UCSC Ensembl
Innerchr9:6691133..6715007hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3823875
hg1923875
hg1823875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758108, nssv3758107
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)nsv1025847
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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