A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997464



Internal ID19157000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..46285hg38UCSC Ensembl
Innerchr3:60333..87967hg19UCSC Ensembl
Innerchr3:35333..62967hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3827631
hg1927635
hg1827635
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4600n100
Supporting Variantsnssv3593485, nssv3593496, nssv3593482, nssv3593489, nssv3593484, nssv3593492, nssv3593481, nssv3593483, nssv3593497, nssv3593494, nssv3593498, nssv3593501, nssv3593495, nssv3593490, nssv3593487, nssv3593486, nssv3593488, nssv3593493, nssv3593499, nssv3593502, nssv3593491, nssv3593500
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)nsv997464
Frequency
Sample Size11257
Observed Gain17
Observed Loss5
Observed Complex0
Frequencyn/a


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