A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002160



Internal ID16948426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:172087622..172088070hg38UCSC Ensembl
Outerchr5:171514626..171515074hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955847
Supporting Variants
SamplesBILGI_BIOE
Known GenesSTK10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002160
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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