A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155103



Internal ID15873851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162054402..162109038hg38UCSC Ensembl
Innerchr6:162475434..162530070hg19UCSC Ensembl
Innerchr6:162395424..162450060hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3854637
hg1954637
hg1854637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605075
Supporting Variants
SamplesHGDP00402
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155103
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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