A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151900



Internal ID15526464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60554932..60743382hg38UCSC Ensembl
Innerchr3:60540665..60729115hg19UCSC Ensembl
Innerchr3:60515705..60704155hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38188451
hg19188451
hg18188451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590406
Supporting Variants
SamplesHGDP00134
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151900
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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