A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607857



Internal ID16395266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:94709551..94942020hg38UCSC Ensembl
Innerchr7:94338863..94571332hg19UCSC Ensembl
Innerchr7:94176799..94409268hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38232470
hg19232470
hg18232470
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11513n54
Supporting Variantsnssv1155857
SamplesNINDS_91
Known GenesPPP1R9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607857
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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