A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612588



Internal ID20985659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18757944..18758473hg38UCSC Ensembl
chr7:18797567..18798096hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155344
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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