A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019599



Internal ID19108817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85773770..85872318hg38UCSC Ensembl
Innerchr7:85403086..85501634hg19UCSC Ensembl
Innerchr7:85241022..85339570hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3898549
hg1998549
hg1898549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6521n100
Supporting Variantsnssv3655179
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)nsv1019599
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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