A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950962



Internal ID16953149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:50076641..50233840hg38UCSC Ensembl
Outerchr10:51836401..51993600hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38157200
hg19157200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997994
SamplesBILGI_BIOE
Known GenesASAH2, FAM21A, FAM21B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950962
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