A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770797



Internal ID18962535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75632863..75636464hg38UCSC Ensembl
chr13:76206999..76210600hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg383602
hg193602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070182
Supporting Variants
SamplesKWP1
Known GenesLMO7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770797
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