A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028941



Internal ID19118160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1109242..1207257hg38UCSC Ensembl
Innerchr7:1148878..1246893hg19UCSC Ensembl
Innerchr7:1115404..1213419hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3898016
hg1998016
hg1898016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654221
Samples
Known GenesC7orf50, ZFAND2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028941
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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