A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866768



Internal ID15814038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10325498..10458952hg38UCSC Ensembl
Innerchr17:10228815..10362269hg19UCSC Ensembl
Innerchr17:10169540..10302994hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38133455
hg19133455
hg18133455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574350
Supporting Variants
Samples
Known GenesMYH13, MYH4, MYH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866768
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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