A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952869



Internal ID16955056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:76787458..76790357hg38UCSC Ensembl
Outerchr14:77253801..77256700hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998374
SamplesBILGI_BIOE
Known GenesANGEL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952869
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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