A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409172



Internal ID21066725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79739559..79742641hg38UCSC Ensembl
chr6:80449276..80452358hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383083
hg193083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147195
Samples
Known GenesRNY4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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