A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454243



Internal ID21111796
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 StatusM
Merged Variants
Supporting Variantsnssv17980026
Samples
Known GenesAKR1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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