A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017890



Internal ID19107107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110073691..110095665hg38UCSC Ensembl
Innerchr6:110394894..110416868hg19UCSC Ensembl
Innerchr6:110501587..110523561hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3821975
hg1921975
hg1821975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6137n100
Supporting Variantsnssv3749511, nssv3654293, nssv3654294, nssv3654292
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)nsv1017890
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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