A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474077



Internal ID251747
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 StatusM
Merged Variants
Supporting Variantsnssv16994779
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474077
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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