A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020080



Internal ID18762616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162324536..162618151hg38UCSC Ensembl
Innerchr6:162745568..163039183hg19UCSC Ensembl
Innerchr6:162665558..162959173hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38293616
hg19293616
hg18293616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6182n100
Supporting Variantsnssv3654608
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)nsv1020080
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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