A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013668



Internal ID22075299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51639362..51644944hg38UCSC Ensembl
Outerchr19:51639099..51651652hg38UCSC Ensembl
Innerchr19:52142615..52148197hg19UCSC Ensembl
Outerchr19:52142352..52154905hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3812554
hg1912554
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155606
Supporting Variants
Samples
Known GenesSIGLEC14
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013668
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer