A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217996



Internal ID20785036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88218201..88222700hg38UCSC Ensembl
chr7:87847516..87852015hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602643
Supporting Variants
Samples
Known GenesSRI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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