A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437402



Internal ID21094955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2974977..2978328hg38UCSC Ensembl
chr11:2996207..2999558hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383352
hg193352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990257
Samples
Known GenesNAP1L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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