A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772396



Internal ID18960738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68610819..68611520hg38UCSC Ensembl
chr12:69004599..69005300hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070535
Supporting Variants
SamplesKWP1
Known GenesRAP1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772396
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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