A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994783



Internal ID63952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40848537..40848587hg38UCSC Ensembl
chr7:40888136..40888186hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493388
Supporting Variants
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994783
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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