A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332722



Internal ID20865896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10962182..10963125hg38UCSC Ensembl
chr1:11022239..11023182hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050823
Samples
Known GenesC1orf127
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332722
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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