A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492376



Internal ID21149929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36999101..36999600hg38UCSC Ensembl
chr13:37573238..37573737hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008393
Samples
Known GenesALG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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