A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443978



Internal ID21101531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3367001..3368200hg38UCSC Ensembl
chr11:3388231..3389430hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990802
Samples
Known GenesZNF195
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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