A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377603



Internal ID21035156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35904920..35909378hg38UCSC Ensembl
chr5:35905022..35909480hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg384459
hg194459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129808
Samples
Known GenesCAPSL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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