A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983847



Internal ID20550887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73081101..73082900hg38UCSC Ensembl
chr10:74840859..74842658hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438877
Supporting Variants
Samples
Known GenesP4HA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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