A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926397



Internal ID22701624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45161872..45163913hg38UCSC Ensembl
chr7:45201471..45203512hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382042
hg192042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445418
Samples
Known GenesRAMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926397
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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