A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136911



Internal ID19278001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:149239887..149240229hg38UCSC Ensembl
Outerchr4:150161039..150161381hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3974821
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136911
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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