A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769675



Internal ID18968685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8481075..8481145hg38UCSC Ensembl
chr17:8384393..8384463hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071332
Supporting Variants
SamplesKWP1
Known GenesMYH10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769675
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer