A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024621



Internal ID19113838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15969743..15990574hg38UCSC Ensembl
Innerchr7:16009368..16030199hg19UCSC Ensembl
Innerchr7:15975893..15996724hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3820832
hg1920832
hg1820832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643188
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)nsv1024621
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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