A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914940



Internal ID22690158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28923734..28924752hg38UCSC Ensembl
chr7:28963351..28964369hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914940
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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