A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3651613



Internal ID18949894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..346365hg38UCSC Ensembl
Innerchr6:257341..346365hg19UCSC Ensembl
Innerchr6:202341..291365hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3889025
hg1989025
hg1889025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032552
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3651613
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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