A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396557



Internal ID21054110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141082713..141083328hg38UCSC Ensembl
chr5:140462294..140462911hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38616
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396557
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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