A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606510



Internal ID20979581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18895494..18896039hg38UCSC Ensembl
chr7:18935117..18935662hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156680
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606510
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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