A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377225



Internal ID21034778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12415729..12716123hg38UCSC Ensembl
chr5:12415841..12716235hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38300395
hg19300395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5643n223
Supporting Variantsnssv18124523
Samples
Known GenesCT49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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