A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462888



Internal ID22520773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127786949..127797376hg38UCSC Ensembl
chr10:129585213..129595640hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3810428
hg1910428
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462888
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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