A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866410



Internal ID16160366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1341698..1405534hg38UCSC Ensembl
Innerchr17:1244992..1308828hg19UCSC Ensembl
Innerchr17:1191742..1255578hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3863837
hg1963837
hg1863837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574209
Supporting Variants
Samples
Known GenesYWHAE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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