A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330490



Internal ID20863647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56738101..56740800hg38UCSC Ensembl
chr1:57203774..57206473hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061742
Samples
Known GenesC1orf168
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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