A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770568



Internal ID19304842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69091409..69091822hg38UCSC Ensembl
chr17:67087550..67087963hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071799
Supporting Variants
SamplesKWP1
Known GenesABCA6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770568
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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