A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327665



Internal ID20860805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197348935..197349988hg38UCSC Ensembl
chr1:197318065..197319118hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056939
Samples
Known GenesCRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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