A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770232



Internal ID18967063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67731296..67731530hg38UCSC Ensembl
chr17:65727412..65727646hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071400
Supporting Variants
SamplesKWP1
Known GenesNOL11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770232
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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