A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154975



Internal ID20722015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2407780..2547870hg38UCSC Ensembl
chr7:2447415..2587504hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38140091
hg19140090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610112
Supporting Variants
Samples
Known GenesBRAT1, CHST12, LFNG, LOC101927181, MIR4648
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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