A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851602



Internal ID22626537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74634393..74640528hg38UCSC Ensembl
chr7:74048709..74054860hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386136
hg196152
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502790
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851602
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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