A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770727



Internal ID18966326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121851729..121852048hg38UCSC Ensembl
chr12:122289635..122289954hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070135
Supporting Variants
SamplesKWP1
Known GenesHPD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770727
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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