A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951916



Internal ID17300790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2850836..2991636hg38UCSC Ensembl
Outerchr1:2767401..2908200hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38140801
hg19140800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998256
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951916
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