A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031665



Internal ID18774199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162177937..162315304hg38UCSC Ensembl
Innerchr6:162598969..162736336hg19UCSC Ensembl
Innerchr6:162518959..162656326hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38137368
hg19137368
hg18137368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749587
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)nsv1031665
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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