A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131424



Internal ID18924548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35105966..35106053hg38UCSC Ensembl
Outerchr19:35596870..35596957hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971261
SamplesKWS1
Known GenesHPN-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131424
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