A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328220



Internal ID20861365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94820001..94820500hg38UCSC Ensembl
chr1:95285557..95286056hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066069
Samples
Known GenesLINC01057, SLC44A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328220
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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