A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952222



Internal ID16954409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:160082711..160099010hg38UCSC Ensembl
Outerchr1:160052501..160068800hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3816300
hg1916300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998279
SamplesBILGI_BIOE
Known GenesIGSF8, KCNJ9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952222
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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