A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602243



Internal ID20975314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18185136..18317655hg38UCSC Ensembl
chr7:18224759..18357278hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38132520
hg19132520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6610n223
Supporting Variantsnssv18154797
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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