A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140500



Internal ID19248887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:2657051..2657120hg38UCSC Ensembl
Outerchr5:2657165..2657234hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957227, nssv3974077
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140500
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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