A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950516



Internal ID16952703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:1663141..1715961hg38UCSC Ensembl
Outerchr1:1594601..1647400hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3852821
hg1952800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997170
SamplesBILGI_BIOE
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950516
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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