A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151337



Internal ID20718377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103456102..103461264hg38UCSC Ensembl
chr7:103096549..103101711hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385163
hg195163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613781
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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