A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399752



Internal ID21057305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57013191..57061645hg38UCSC Ensembl
chr6:56877989..56926443hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3848455
hg1948455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144794
Samples
Known GenesBEND6, KIAA1586
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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