A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024763



Internal ID19113980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7022554..7061314hg38UCSC Ensembl
Innerchr9:7022554..7061314hg19UCSC Ensembl
Innerchr9:7012554..7051314hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3838761
hg1938761
hg1838761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689102
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)nsv1024763
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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