A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748244



Internal ID16042200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:53874530..53902466hg38UCSC Ensembl
Innerchr10:55634290..55662226hg19UCSC Ensembl
Innerchr10:55304296..55332232hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3827937
hg1927937
hg1827937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550947
Supporting Variants
Samples
Known GenesPCDH15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv748244
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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