A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072396



Internal ID15925582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:124355570..124371871hg38UCSC Ensembl
Innerchr6:124676716..124693017hg19UCSC Ensembl
Innerchr6:124718415..124734716hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3816302
hg1916302
hg1816302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604598
Supporting Variants
Samples
Known GenesNKAIN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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