A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028090



Internal ID19117308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91446783..91524387hg38UCSC Ensembl
Innerchr7:91076098..91153702hg19UCSC Ensembl
Innerchr7:90914034..90991638hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3877605
hg1977605
hg1877605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655241
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)nsv1028090
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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