A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019900



Internal ID18762435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162238004..162421445hg38UCSC Ensembl
Innerchr6:162659036..162842477hg19UCSC Ensembl
Innerchr6:162579026..162762467hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38183442
hg19183442
hg18183442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6180n100
Supporting Variantsnssv3654567
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)nsv1019900
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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