A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938599



Internal ID15885869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19231033..19273047hg38UCSC Ensembl
Innerchr20:19211677..19253691hg19UCSC Ensembl
Innerchr20:19159677..19201691hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3842015
hg1942015
hg1842015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585671
Supporting Variants
Samples
Known GenesLOC100130264, SLC24A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938599
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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