A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611829



Internal ID20984900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96913071..96948860hg38UCSC Ensembl
chr6:97360947..97396736hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3835790
hg1935790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150513
Samples
Known GenesKLHL32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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