A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612857



Internal ID20985928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143630070..143638470hg38UCSC Ensembl
chr6:143951207..143959607hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg388401
hg198401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140245
Samples
Known GenesPHACTR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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