A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137969



Internal ID19277050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125897168..125897228hg38UCSC Ensembl
Outerchr10:127585737..127585797hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990499
SamplesKWS2
Known GenesFANK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137969
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