A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926520



Internal ID22701747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2762249..2762298hg38UCSC Ensembl
chr7:2801883..2801932hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436247
Samples
Known GenesGNA12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926520
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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