A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1070568



Internal ID15923754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100624431..100750077hg38UCSC Ensembl
Innerchr6:101072307..101197953hg19UCSC Ensembl
Innerchr6:101179028..101304674hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38125647
hg19125647
hg18125647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604273
Supporting Variants
Samples
Known GenesASCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1070568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer