A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492138



Internal ID21149691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29947501..29949300hg38UCSC Ensembl
chr13:30521638..30523437hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007881
Samples
Known GenesLINC00544
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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