A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657456



Internal ID18609051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52376160..52417602hg38UCSC Ensembl
Innerchr6:52240958..52282400hg19UCSC Ensembl
Innerchr6:52348917..52390359hg18UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3841443
hg1941443
hg1841443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027645
Supporting Variants
Samples
Known GenesPAQR8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657456
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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