A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028583



Internal ID19117801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100643558..100704755hg38UCSC Ensembl
Innerchr6:101091434..101152631hg19UCSC Ensembl
Innerchr6:101198155..101259352hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3861198
hg1961198
hg1861198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6113n100
Supporting Variantsnssv3649857
Samples
Known GenesASCC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028583
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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