A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958049



Internal ID15905319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4231805..4473507hg38UCSC Ensembl
Innerchr3:4273489..4515191hg19UCSC Ensembl
Innerchr3:4248489..4490191hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38241703
hg19241703
hg18241703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589451
Supporting Variants
Samples
Known GenesSETMAR, SUMF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv958049
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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