A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110160



Internal ID19259317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:7564837..7565937hg38UCSC Ensembl
Outerchr10:7606800..7607900hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959427
SamplesKWS1
Known GenesITIH5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110160
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