A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031355



Internal ID18773889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162550516..162619009hg38UCSC Ensembl
Innerchr6:162971548..163040041hg19UCSC Ensembl
Innerchr6:162891538..162960031hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3868494
hg1968494
hg1868494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6192n100
Supporting Variantsnssv3655380
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)nsv1031355
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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