A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360420



Internal ID22586089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58211901..58211901hg38UCSC Ensembl
chr10:59971662..59971662hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959708
Supporting Variants
Samples
Known GenesIPMK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360420
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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