A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604401



Internal ID20977472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116580701..116582600hg38UCSC Ensembl
chr6:116901864..116903763hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137158
Samples
Known GenesRWDD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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