A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1010001



Internal ID15957271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160673871..161986681hg38UCSC Ensembl
Innerchr4:161595023..162907833hg19UCSC Ensembl
Innerchr4:161814473..163127283hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381312811
hg191312811
hg181312811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595875
Supporting Variants
Samples
Known GenesFSTL5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1010001
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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