A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576033



Internal ID16016756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75592461..75623840hg38UCSC Ensembl
Innerchr17:73588542..73619920hg19UCSC Ensembl
Innerchr17:71100137..71131515hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3831380
hg1931379
hg1831379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149810
SamplesHGDP01048
Known GenesMYO15B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576033
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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