A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070225



Internal ID19316978
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 StatusM
Merged Variants
Supporting Variantsnssv3765024
SamplesKWP1
Known GenesCHURC1-FNTB, FNTB, MAX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070225
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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