A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124625



Internal ID19272807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:108310442..108316542hg38UCSC Ensembl
Outerchr10:110070200..110076300hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976679
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124625
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