A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118105



Internal ID18903086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:22142407..22143707hg38UCSC Ensembl
Outerchr1:22468900..22470200hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv57n106
Supporting Variantsnssv3980324
SamplesKWS1
Known GenesWNT4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118105
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