A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004457



Internal ID19093675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28499816..28553820hg38UCSC Ensembl
Innerchr3:28541307..28595311hg19UCSC Ensembl
Innerchr3:28516311..28570315hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3854005
hg1954005
hg1854005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589568
Samples
Known GenesZCWPW2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004457
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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