A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118794



Internal ID19268727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35170165..35174930hg38UCSC Ensembl
Outerchr19:35661068..35665833hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg384766
hg194766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1774n106
Supporting Variantsnssv3981106
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118794
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