A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994779



Internal ID63949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40811630..40811785hg38UCSC Ensembl
chr7:40851229..40851384hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474077
Supporting Variants
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994779
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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