A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576029



Internal ID16016752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75546948..75566796hg38UCSC Ensembl
Innerchr17:73543029..73562877hg19UCSC Ensembl
Innerchr17:71054624..71074472hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3819849
hg1919849
hg1819849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876106
Samples
Known GenesLLGL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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