A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528172



Internal ID20901533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38003608..38004174hg38UCSC Ensembl
chr19:38494248..38494814hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046704
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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