A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072696



Internal ID18977469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63863823..63864124hg38UCSC Ensembl
chr3:63849499..63849800hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771379
SamplesKWP1
Known GenesTHOC7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072696
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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