A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576189



Internal ID16016912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82050142..82056985hg38UCSC Ensembl
Innerchr17:80008018..80014861hg19UCSC Ensembl
Innerchr17:77601307..77608150hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg386844
hg196844
hg186844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877122
Samples
Known GenesGPS1, RFNG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576189
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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