A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952837



Internal ID17301711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:50928383..50946182hg38UCSC Ensembl
Outerchr14:51395101..51412900hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3817800
hg1917800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998338
SamplesBILGI_BIOE
Known GenesPYGL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952837
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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