A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654554



Internal ID18606149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162148169..162269734hg38UCSC Ensembl
Innerchr6:162569201..162690766hg19UCSC Ensembl
Innerchr6:162489191..162610756hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38121566
hg19121566
hg18121566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027860
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)nssv3654554
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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