A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848191



Internal ID22623126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145907479..145908657hg38UCSC Ensembl
chr7:145604572..145605750hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502198, nssv17502197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848191
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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