A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865830



Internal ID22640765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81743101..81745275hg38UCSC Ensembl
chr7:81372417..81374591hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382175
hg192175
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503487
Samples
Known GenesHGF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865830
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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