A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029749



Internal ID18772280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161543443..162045027hg38UCSC Ensembl
Innerchr6:161964475..162466059hg19UCSC Ensembl
Innerchr6:161884465..162386049hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38501585
hg19501585
hg18501585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654531, nssv3654532
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)nsv1029749
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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