A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952099



Internal ID16954286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:215081958..215084157hg38UCSC Ensembl
Outerchr1:215255301..215257500hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000218
SamplesBILGI_BIOE
Known GenesKCNK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952099
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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