A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387239



Internal ID21044792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171526776..171713994hg38UCSC Ensembl
chr4:172447927..172635145hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38187219
hg19187219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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