A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006678



Internal ID19095896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28917720..28973263hg38UCSC Ensembl
Innerchr3:28959211..29014754hg19UCSC Ensembl
Innerchr3:28934215..28989758hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3855544
hg1955544
hg1855544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4714n100
Supporting Variantsnssv3589576, nssv3589577, nssv3589578
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)nsv1006678
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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