A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853175



Internal ID22628110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73081198..73082828hg38UCSC Ensembl
chr10:74840956..74842586hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381631
hg191631
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456702
Samples
Known GenesP4HA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853175
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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