A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769977



Internal ID18968089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:17132480..17132536hg38UCSC Ensembl
chr16:17226337..17226393hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071271
Supporting Variants
SamplesKWP1
Known GenesXYLT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769977
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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