A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150187



Internal ID20717227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124571701..124574500hg38UCSC Ensembl
chr7:124211755..124214554hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00065


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