A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387577



Internal ID21045130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139214901..139222219hg38UCSC Ensembl
chr4:140136055..140143373hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg387319
hg197319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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