A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606563



Internal ID20979634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105033920..105037004hg38UCSC Ensembl
chr7:104674367..104677451hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg383085
hg193085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152024
Samples
Known GenesKMT2E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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