A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126502



Internal ID18908080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1802001..1802501hg38UCSC Ensembl
Outerchr19:1802000..1802500hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984754
SamplesKWS1
Known GenesATP8B3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126502
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