A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135570



Internal ID19264625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:11536617..11536940hg38UCSC Ensembl
Outerchr20:11517265..11517588hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2213n106
Supporting Variantsnssv3965695, nssv3989958
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135570
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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