A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141173



Internal ID19276098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:41837009..41885273hg38UCSC Ensembl
Outerchr10:42354900..42403200hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3848265
hg1948301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv411n106
Supporting Variantsnssv3992680
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141173
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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