A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769655



Internal ID19312682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:58451974..58452151hg38UCSC Ensembl
chr12:58845757..58845934hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071037
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769655
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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