A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159438



Internal ID20726478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73368744..73371855hg38UCSC Ensembl
chr7:72782738..72785849hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383112
hg193112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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