A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861591



Internal ID22636526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73755112..73757911hg38UCSC Ensembl
chr7:73169442..73172241hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509300, nssv17502761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861591
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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