A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950723



Internal ID17299597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:176719400..176750099hg38UCSC Ensembl
Outerchr5:176146401..176177100hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3830700
hg1930700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997895
SamplesBILGI_BIOE
Known GenesLOC102577424
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950723
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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