A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654603



Internal ID18606198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162307914..162474720hg38UCSC Ensembl
Innerchr6:162728946..162895752hg19UCSC Ensembl
Innerchr6:162648936..162815742hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38166807
hg19166807
hg18166807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016161
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3654603
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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