A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv876105



Internal ID15823375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75526859..75546743hg38UCSC Ensembl
Innerchr17:73522940..73542824hg19UCSC Ensembl
Innerchr17:71034535..71054419hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3819885
hg1919885
hg1819885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576028
Supporting Variants
Samples
Known GenesLLGL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv876105
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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