A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952821



Internal ID17301695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:26632495..26674394hg38UCSC Ensembl
Outerchr14:27101701..27143600hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3841900
hg1941900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998320
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952821
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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