A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915348



Internal ID22690566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67752503..67758010hg38UCSC Ensembl
chr7:67217490..67222997hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg385508
hg195508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915348
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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