A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958738



Internal ID17307611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:31344683..31344844hg38UCSC Ensembl
Outerchr14:31813889..31814050hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005412
SamplesBILGI_BIOE
Known GenesHEATR5A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958738
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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