A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020148



Internal ID19109367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91709837..91729627hg38UCSC Ensembl
Innerchr7:91339152..91358942hg19UCSC Ensembl
Innerchr7:91177088..91196878hg18UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3819791
hg1919791
hg1819791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655244
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)nsv1020148
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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