A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958507



Internal ID17307380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:39150879..39150948hg38UCSC Ensembl
Outerchr8:39008398..39008467hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001222
SamplesBILGI_BIOE
Known GenesADAM32
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958507
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