A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375017



Internal ID21032570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188009726..188010692hg38UCSC Ensembl
chr3:187727514..187728480hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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