A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985201



Internal ID18876320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:37187223..37187519hg38UCSC Ensembl
Outerchr20:35815626..35815922hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126922
Supporting Variants
SamplesKWS1
Known GenesRPN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985201
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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