A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765024



Internal ID19305272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65060428..65060708hg38UCSC Ensembl
chr14:65527146..65527426hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070225
Supporting Variants
SamplesKWP1
Known GenesCHURC1-FNTB, FNTB, MAX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765024
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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