A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950599



Internal ID17299473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:34569200..34574299hg38UCSC Ensembl
Outerchr1:35034801..35039900hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997123
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950599
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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