A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912327



Internal ID22687543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29525749..29525802hg38UCSC Ensembl
chr7:29565365..29565418hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440990
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912327
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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