A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611693



Internal ID20984764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144587229..144587992hg38UCSC Ensembl
chr6:144908365..144909128hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38764
hg19764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140287
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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