A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769899



Internal ID19311874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92730042..92730743hg38UCSC Ensembl
chr10:94489799..94490500hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070881
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769899
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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