A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966736



Internal ID22741671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104735456..104735456hg38UCSC Ensembl
chr10:106495214..106495214hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360471
Samples
Known GenesSORCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966736
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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