A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150119



Internal ID20717159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124008785..124027277hg38UCSC Ensembl
chr7:123648839..123667331hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3818493
hg1918493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610715
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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