A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154848



Internal ID20721888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2263653..2302392hg38UCSC Ensembl
chr7:2303288..2342027hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3838740
hg1938740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600445
Supporting Variants
Samples
Known GenesSNX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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