A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654555



Internal ID18606150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162150231..162169397hg38UCSC Ensembl
Innerchr6:162571263..162590429hg19UCSC Ensembl
Innerchr6:162491253..162510419hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3819167
hg1919167
hg1819167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032437
Supporting Variants
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)nssv3654555
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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