A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000064



Internal ID17293016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:27804680..27805879hg38UCSC Ensembl
Outerchr16:27816001..27817200hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952960
Supporting Variants
SamplesBILGI_BIOE
Known GenesGSG1L
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000064
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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