A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479014



Internal ID256554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156994381..156994529hg38UCSC Ensembl
chr7:156787075..156787223hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005995
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479014
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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