A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866029



Internal ID16159985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948888..949861hg38UCSC Ensembl
Innerchr17:852128..853101hg19UCSC Ensembl
Innerchr17:798878..799851hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38974
hg19974
hg18974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574109
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)nssv866029
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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