A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423818



Internal ID21081371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138921806..138931625hg38UCSC Ensembl
chr7:138606552..138616371hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg389820
hg199820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155234
Samples
Known GenesKIAA1549
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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