A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023149



Internal ID19112366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81188234..81298774hg38UCSC Ensembl
Innerchr7:80817550..80928090hg19UCSC Ensembl
Innerchr7:80655486..80766026hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38110541
hg19110541
hg18110541
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655146
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)nsv1023149
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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