A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526852



Internal ID20900213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37974941..38004078hg38UCSC Ensembl
chr19:38465581..38494718hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3829138
hg1929138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046700
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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