A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388621



Internal ID21046174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140321619..140326129hg38UCSC Ensembl
chr4:141242773..141247283hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg384511
hg194511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108100
Samples
Known GenesLOC100129858, SCOC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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