A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848738



Internal ID22623673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145970912..145973133hg38UCSC Ensembl
chr7:145668005..145670226hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg382222
hg192222
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502201, nssv17502202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848738
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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