A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999225



Internal ID17292177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14686944..14712843hg38UCSC Ensembl
Outerchr16:14780801..14806700hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3825900
hg1925900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952927
Supporting Variants
SamplesBILGI_BIOE
Known GenesNPIPA2, NPIPA3, PLA2G10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999225
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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