A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654537



Internal ID18606132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161809542..162125672hg38UCSC Ensembl
Innerchr6:162230574..162546704hg19UCSC Ensembl
Innerchr6:162150564..162466694hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38316131
hg19316131
hg18316131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018409
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)nssv3654537
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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