A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424540



Internal ID21082093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91303863..91330865hg38UCSC Ensembl
chr8:92316091..92343093hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3827003
hg1927003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234279
Samples
Known GenesSLC26A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424540
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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