A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931860



Internal ID21351929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38123801..38123879hg38UCSC Ensembl
chr19:38614441..38614519hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177381
SamplesHG002
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931860
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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