A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957443



Internal ID19219881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:2748610..2748746hg38UCSC Ensembl
Outerchr4:2750337..2750473hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128023
Supporting Variants
SamplesKWS1
Known GenesTNIP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957443
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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