A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990400



Internal ID18879476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13115031..13115106hg38UCSC Ensembl
Outerchr10:13157031..13157106hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137877
Supporting Variants
SamplesKWS2
Known GenesOPTN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990400
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