A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1048513



Internal ID15555013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:666725..667538hg38UCSC Ensembl
Innerchr6:666725..667538hg19UCSC Ensembl
Innerchr6:611725..612538hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38814
hg19814
hg18814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600797
Supporting Variants
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1048513
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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