A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154831



Internal ID20721871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18416550..18444150hg38UCSC Ensembl
chr7:18456173..18483773hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3827601
hg1927601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618195
Supporting Variants
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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