A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544345



Internal ID20917585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36485455..36490635hg38UCSC Ensembl
chr21:37857753..37862933hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg385181
hg195181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203940
Samples
Known GenesCLDN14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544345
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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