A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119002



Internal ID18917004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:68304882..68474682hg38UCSC Ensembl
Outerchr4:69170600..69340400hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38169801
hg19169801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981796
SamplesKWS1
Known GenesTMPRSS11E, YTHDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119002
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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