A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153960



Internal ID20721000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148475746..148476626hg38UCSC Ensembl
chr7:148172838..148173718hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432152
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153960
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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