A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914713



Internal ID22689930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37653835..37665531hg38UCSC Ensembl
chr7:37693438..37705134hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3811697
hg1911697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914713
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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