A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326269



Internal ID20859403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11916309..11929501hg38UCSC Ensembl
chr1:11976366..11989558hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3813193
hg1913193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051245
Samples
Known GenesKIAA2013
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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