A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955453



Internal ID16957640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:92785954..92786095hg38UCSC Ensembl
Outerchr1:93251511..93251652hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000540
SamplesBILGI_BIOE
Known GenesEVI5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955453
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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