A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877271



Internal ID16171227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82974920..83004371hg38UCSC Ensembl
Innerchr17:80932796..80962247hg19UCSC Ensembl
Innerchr17:78526085..78555536hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3829452
hg1929452
hg1829452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576218
Supporting Variants
Samples
Known GenesB3GNTL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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