A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075557



Internal ID15582057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162379124..163058475hg38UCSC Ensembl
Innerchr6:162800156..163479507hg19UCSC Ensembl
Innerchr6:162720146..163399497hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38679352
hg19679352
hg18679352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605159
Supporting Variants
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075557
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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