A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527363



Internal ID20900724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38161102..38176711hg38UCSC Ensembl
chr19:38651742..38667351hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3815610
hg1915610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046711
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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