A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426261



Internal ID21083814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11942777..12450883hg38UCSC Ensembl
chr9:11942777..12450883hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38508107
hg19508107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7597n223
Supporting Variantsnssv18176220
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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