A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872252



Internal ID15819522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45512721..45518744hg38UCSC Ensembl
Innerchr17:43590087..43596110hg19UCSC Ensembl
Innerchr17:40945870..40951893hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg386024
hg196024
hg186024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575112
Supporting Variants
Samples
Known GenesLRRC37A4P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872252
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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