A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387591



Internal ID21045144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99508201..99518500hg38UCSC Ensembl
chr4:100429358..100439657hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121324
Samples
Known GenesC4orf17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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