A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570827



Internal ID16011550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100884530..100924371hg38UCSC Ensembl
Innerchr15:101424735..101464576hg19UCSC Ensembl
Innerchr15:99242258..99282099hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3839842
hg1939842
hg1839842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148889
SamplesHGDP01012
Known GenesALDH1A3, LRRK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570827
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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