A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154766



Internal ID20721806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17890301..17891700hg38UCSC Ensembl
chr7:17929924..17931323hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606776
Supporting Variants
Samples
Known GenesSNX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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