A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159466



Internal ID20726506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73692163..73694338hg38UCSC Ensembl
chr7:73106493..73108668hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382176
hg192176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604545
Supporting Variants
Samples
Known GenesWBSCR22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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