A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109039



Internal ID19285320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:16124707..16125375hg38UCSC Ensembl
Outerchr5:16124816..16125484hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3048n106
Supporting Variantsnssv3954874
SamplesKWS1
Known GenesMARCH11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109039
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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