A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072365



Internal ID15925551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123271188..123271795hg38UCSC Ensembl
Innerchr6:123592333..123592940hg19UCSC Ensembl
Innerchr6:123634032..123634639hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38608
hg19608
hg18608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604577
Supporting Variants
Samples
Known GenesTRDN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072365
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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