A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075186



Internal ID15928372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160836386..160849587hg38UCSC Ensembl
Innerchr6:161257418..161270619hg19UCSC Ensembl
Innerchr6:161177408..161190609hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3813202
hg1913202
hg1813202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605011
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075186
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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