A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608233



Internal ID20981304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18121700..18140975hg38UCSC Ensembl
chr7:18161323..18180598hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3819276
hg1919276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154791
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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