A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028799



Internal ID19118017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62553935..63232853hg38UCSC Ensembl
Innerchr7:62014313..62693231hg19UCSC Ensembl
Innerchr7:61651748..62330666hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38678919
hg19678919
hg18678919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6411n100
Supporting Variantsnssv3661834
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)nsv1028799
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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