A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002968



Internal ID19092185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165541222..165579315hg38UCSC Ensembl
Innerchr3:165259010..165297103hg19UCSC Ensembl
Innerchr3:166741704..166779797hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3838094
hg1938094
hg1838094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4973n100
Supporting Variantsnssv3612553, nssv3612574, nssv3612565, nssv3612564, nssv3612575, nssv3612561, nssv3612577, nssv3612556, nssv3612563, nssv3612570, nssv3612555, nssv3612554, nssv3612569, nssv3612576, nssv3612566, nssv3612559, nssv3612558, nssv3612573, nssv3612557, nssv3612581, nssv3612580, nssv3612560, nssv3612571, nssv3612572, nssv3612568, nssv3612578, nssv3612567, nssv3612562, nssv3612579
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)nsv1002968
Frequency
Sample Size11257
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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