A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576222



Internal ID16363631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:83028664..83077947hg38UCSC Ensembl
Innerchr17:80986540..81035823hg19UCSC Ensembl
Innerchr17:78579829..78629112hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3849284
hg1949284
hg1849284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877275
Samples
Known GenesB3GNTL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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