A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589567



Internal ID18887848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28167185..28210540hg38UCSC Ensembl
Innerchr3:28208676..28252031hg19UCSC Ensembl
Innerchr3:28183680..28227035hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3843356
hg1943356
hg1843356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998002
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589567
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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