A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327370



Internal ID20860508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:120955874..120959780hg38UCSC Ensembl
chr1:144294195..144298101hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg383907
hg193907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051305
Samples
Known GenesLOC100288142
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327370
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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