A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953972



Internal ID17302846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9784925..9794824hg38UCSC Ensembl
Outerchr19:9895601..9905500hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998950
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953972
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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