A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771178



Internal ID19306420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1825998..1826699hg38UCSC Ensembl
chr16:1875999..1876700hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070733
Supporting Variants
SamplesKWP1
Known GenesHAGH
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771178
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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