A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075376



Internal ID15581876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161393875..161438978hg38UCSC Ensembl
Innerchr6:161814907..161860010hg19UCSC Ensembl
Innerchr6:161734897..161780000hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3845104
hg1945104
hg1845104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605066
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075376
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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