A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398804



Internal ID21056357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126486505..126486822hg38UCSC Ensembl
chr5:125822197..125822514hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124293
Samples
Known GenesGRAMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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