A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907653



Internal ID22682863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85174852..85183001hg38UCSC Ensembl
chr7:84804168..84812317hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg388150
hg198150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907653
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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