A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575504



Internal ID16362913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:49747243..49750286hg38UCSC Ensembl
Innerchr17:47824605..47827648hg19UCSC Ensembl
Innerchr17:45179604..45182647hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg383044
hg193044
hg183044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv873310
Samples
Known GenesFAM117A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575504
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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