A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374122



Internal ID21031675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17354452..17354945hg38UCSC Ensembl
chr4:17356075..17356568hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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