A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145065



Internal ID19277328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:77077075..77077675hg38UCSC Ensembl
Outerchr5:76372900..76373500hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981684
SamplesKWS1
Known GenesZBED3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145065
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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