A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973931



Internal ID18886584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:39475023..39475077hg38UCSC Ensembl
Outerchr4:39476643..39476697hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123777
Supporting Variants
SamplesKWS2
Known GenesLIAS, MIR1273H
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973931
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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