A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589574



Internal ID18887855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28917720..28958686hg38UCSC Ensembl
Innerchr3:28959211..29000177hg19UCSC Ensembl
Innerchr3:28934215..28975181hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3840967
hg1940967
hg1840967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004914
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)nssv3589574
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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