A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952398



Internal ID17301272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:83049325..83129630hg38UCSC Ensembl
Outerchr17:81007201..81077400hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3880306
hg1970200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998831
SamplesBILGI_BIOE
Known GenesB3GNTL1, METRNL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952398
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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