A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005603



Internal ID17298555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20767239..20767539hg38UCSC Ensembl
Outerchr16:20778561..20778861hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958185
Supporting Variants
SamplesBILGI_BIOE
Known GenesACSM3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005603
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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