A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989779



Internal ID18891154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:73059462..73060362hg38UCSC Ensembl
Outerchr13:73633600..73634500hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136172
Supporting Variants
SamplesKWS2
Known GenesKLF5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989779
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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