A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152038



Internal ID20719078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105285123..105286999hg38UCSC Ensembl
chr7:104925570..104927446hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381877
hg191877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615611
Supporting Variants
Samples
Known GenesSRPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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