A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077312



Internal ID15930498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168316451..168319244hg38UCSC Ensembl
Innerchr6:168717131..168719924hg19UCSC Ensembl
Innerchr6:168459980..168462773hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382794
hg192794
hg182794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605466
Supporting Variants
Samples
Known GenesDACT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077312
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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