A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159459



Internal ID20726499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73612541..73615812hg38UCSC Ensembl
chr7:73026871..73030142hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383272
hg193272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605858
Supporting Variants
Samples
Known GenesMLXIPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159459
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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