A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999171



Internal ID19158707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..66756hg38UCSC Ensembl
Innerchr3:60333..108439hg19UCSC Ensembl
Innerchr3:35333..83439hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3848102
hg1948107
hg1848107
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4603n100
Supporting Variantsnssv3593520, nssv3593514, nssv3593516, nssv3593517, nssv3593515, nssv3593512, nssv3593513, nssv3593519, nssv3593518
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)nsv999171
Frequency
Sample Size11257
Observed Gain8
Observed Loss1
Observed Complex0
Frequencyn/a


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