A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401913



Internal ID21059466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89435980..89436491hg38UCSC Ensembl
chr6:90145699..90146210hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148101
Samples
Known GenesANKRD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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