A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327938



Internal ID20861082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94663401..94690600hg38UCSC Ensembl
chr1:95128957..95156156hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3827200
hg1927200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv272n223
Supporting Variantsnssv18065643
Samples
Known GenesLINC01057
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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