A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029592



Internal ID18772123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162021850..162638395hg38UCSC Ensembl
Innerchr6:162442882..163059427hg19UCSC Ensembl
Innerchr6:162362872..162979417hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38616546
hg19616546
hg18616546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654546
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)nsv1029592
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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