A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772837



Internal ID18959138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121466196..121467597hg38UCSC Ensembl
chr12:121903999..121905400hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070134
Supporting Variants
SamplesKWP1
Known GenesKDM2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772837
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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