A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380891



Internal ID21038444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7836786..7842087hg38UCSC Ensembl
chr5:7836899..7842200hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385302
hg195302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133960
Samples
Known GenesC5orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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