A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954733



Internal ID17303606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:177399087..177399142hg38UCSC Ensembl
Outerchr1:177368223..177368278hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000494
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954733
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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