A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654542



Internal ID18952823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161925250..162141466hg38UCSC Ensembl
Innerchr6:162346282..162562498hg19UCSC Ensembl
Innerchr6:162266272..162482488hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38216217
hg19216217
hg18216217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022804
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)nssv3654542
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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