A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032729



Internal ID20599769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75624375..75634810hg38UCSC Ensembl
chr16:75658273..75668708hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3810436
hg1910436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496833
Supporting Variants
Samples
Known GenesKARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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