A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997703



Internal ID17290655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:10454289..10465188hg38UCSC Ensembl
Outerchr5:10454401..10465300hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950647
Supporting Variants
SamplesBILGI_BIOE
Known GenesROPN1L
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997703
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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