A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610896



Internal ID20983967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110847301..110848400hg38UCSC Ensembl
chr6:111168504..111169603hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135385
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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