A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004914



Internal ID19094131
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 StatusM
Merged Variantsdgv4713n100
Supporting Variantsnssv3589571, nssv3589572, nssv3739665, nssv3589574, nssv3589573, nssv3589575
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)nsv1004914
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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