A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952397



Internal ID17301271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:83002425..83012524hg38UCSC Ensembl
Outerchr17:80960301..80970400hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998830
SamplesBILGI_BIOE
Known GenesB3GNTL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952397
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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