A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576221



Internal ID16363630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:83022441..83023178hg38UCSC Ensembl
Innerchr17:80980317..80981054hg19UCSC Ensembl
Innerchr17:78573606..78574343hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38738
hg19738
hg18738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5807n54
Supporting Variantsnssv877274
Samples
Known GenesB3GNTL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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