A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969522



Internal ID18879818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:38663479..38665179hg38UCSC Ensembl
Outerchr4:38665100..38666800hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122085
Supporting Variants
SamplesKWS2
Known GenesFLJ13197, KLF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969522
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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