A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435869



Internal ID21093422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31398901..31448188hg38UCSC Ensembl
chr11:31420448..31469735hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3849288
hg1949288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989653
Samples
Known GenesDNAJC24, IMMP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435869
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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