A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378287



Internal ID21035840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97509228..97661211hg38UCSC Ensembl
chr4:98430379..98582362hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38151984
hg19151984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121530
Samples
Known GenesSTPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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