A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952377



Internal ID17301251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:78923019..78984118hg38UCSC Ensembl
Outerchr17:76919101..76980200hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3861100
hg1961100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998810
SamplesBILGI_BIOE
Known GenesLGALS3BP, TIMP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952377
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer