A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393276



Internal ID21050829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44095864..44096234hg38UCSC Ensembl
chr4:44097881..44098251hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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