A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386088



Internal ID21043641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176906412..176906634hg38UCSC Ensembl
chr4:177827566..177827788hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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