A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592128



Internal ID16032851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:160795732..161829856hg38UCSC Ensembl
Innerchr3:160513520..161547644hg19UCSC Ensembl
Innerchr3:161996214..163030338hg18UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg381034125
hg191034125
hg181034125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv977323
Samples
Known GenesB3GALNT1, LOC101243545, NMD3, OTOL1, PPM1L, SPTSSB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592128
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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