A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939506



Internal ID15886776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42668354..42752575hg38UCSC Ensembl
Innerchr20:41296994..41381215hg19UCSC Ensembl
Innerchr20:40730408..40814629hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3884222
hg1984222
hg1884222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586028
Supporting Variants
Samples
Known GenesPTPRT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939506
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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