A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023416



Internal ID19112633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..291070hg38UCSC Ensembl
Innerchr6:257341..291070hg19UCSC Ensembl
Innerchr6:202341..236070hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3833730
hg1933730
hg1833730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5879n100
Supporting Variantsnssv3650465, nssv3650467, nssv3746775, nssv3650468, nssv3746776, nssv3650469, nssv3650464, nssv3650466
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)nsv1023416
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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