A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704257



Internal ID21376533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123996875..123997205hg38UCSC Ensembl
chr7:123636929..123637259hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388669
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704257
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0287356


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