A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608590



Internal ID16049313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142136069..142240255hg38UCSC Ensembl
Innerchr7:141835869..141940073hg19UCSC Ensembl
Innerchr7:141482338..141586547hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38104187
hg19104205
hg18104210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1095741
Samples
Known GenesLOC93432
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608590
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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