A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915311



Internal ID22690529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119818790..120155724hg38UCSC Ensembl
chr7:119458844..119795778hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38336935
hg19336935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915311
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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