A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768280



Internal ID19308430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77220856..77221657hg38UCSC Ensembl
chr14:77687199..77688000hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069806
Supporting Variants
SamplesKWP1
Known GenesTMEM63C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768280
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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