A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017053



Internal ID18759588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162344133..162580790hg38UCSC Ensembl
Innerchr6:162765165..163001822hg19UCSC Ensembl
Innerchr6:162685155..162921812hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38236658
hg19236658
hg18236658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6182n100
Supporting Variantsnssv3654609
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)nsv1017053
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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