A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335305



Internal ID20868497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89996945..90004195hg38UCSC Ensembl
chr1:90462504..90469754hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg387251
hg197251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064961
Samples
Known GenesZNF326
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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