A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436702



Internal ID21094255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126283024..126288934hg38UCSC Ensembl
chr9:129045303..129051213hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385911
hg195911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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