A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1114691



Internal ID19266684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:72946704..72946778hg38UCSC Ensembl
Outerchr5:72242531..72242605hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3974598
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1114691
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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