A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769075



Internal ID18966864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10764782..10764916hg38UCSC Ensembl
chr16:10858639..10858773hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070327
Supporting Variants
SamplesKWP1
Known GenesNUBP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769075
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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