A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376731



Internal ID21034284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53229803..53252919hg38UCSC Ensembl
chr4:54095970..54119086hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3823117
hg1923117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117399
Samples
Known GenesSCFD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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