A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926470



Internal ID22701697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156994381..156994526hg38UCSC Ensembl
chr7:156787075..156787220hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926470
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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