A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960432



Internal ID19209174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131109637..131115537hg38UCSC Ensembl
Outerchr10:132907900..132913800hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385901
hg195901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128533
Supporting Variants
SamplesKWS1
Known GenesTCERG1L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960432
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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