A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866127



Internal ID16160083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948992..952193hg38UCSC Ensembl
Innerchr17:852232..855433hg19UCSC Ensembl
Innerchr17:798982..802183hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383202
hg193202
hg183202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574123
Supporting Variants
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866127
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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