A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015465



Internal ID19104682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100643558..100709617hg38UCSC Ensembl
Innerchr6:101091434..101157493hg19UCSC Ensembl
Innerchr6:101198155..101264214hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3866060
hg1966060
hg1866060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6113n100
Supporting Variantsnssv3649858
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)nsv1015465
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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