A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028918



Internal ID18771450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161893522..161949740hg38UCSC Ensembl
Innerchr6:162314554..162370772hg19UCSC Ensembl
Innerchr6:162234544..162290762hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3856219
hg1956219
hg1856219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654539
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)nsv1028918
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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