A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025023



Internal ID18767555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:17826173..18318007hg38UCSC Ensembl
Innerchr7:17865796..18357630hg19UCSC Ensembl
Innerchr7:17832321..18324155hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38491835
hg19491835
hg18491835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643231
Samples
Known GenesHDAC9, PRPS1L1, SNX13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025023
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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