A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018013



Internal ID19107230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61081237..62835849hg38UCSC Ensembl
Innerchr7:61063962..62296227hg19UCSC Ensembl
Innerchr7:61067904..61933662hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381754613
hg191232266
hg18865759
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6386n100
Supporting Variantsnssv3661545
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018013
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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