A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950521



Internal ID16952708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:1729062..1760461hg38UCSC Ensembl
Outerchr1:1660501..1691900hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3831400
hg1931400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997181
SamplesBILGI_BIOE
Known GenesNADK, SLC35E2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950521
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