A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573876



Internal ID16014599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:170860..178833hg38UCSC Ensembl
Innerchr17:20651..28624hg19UCSC Ensembl
Innerchr17:20651..28624hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg387974
hg197974
hg187974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv864142
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573876
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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