A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980026



Internal ID20547066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4952198..4970252hg38UCSC Ensembl
chr10:4994390..5012444hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3818055
hg1918055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454243
Supporting Variants
Samples
Known GenesAKR1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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