A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769850



Internal ID19307892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70211266..70211407hg38UCSC Ensembl
chr3:70260417..70260558hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074600
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769850
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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