A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321268



Internal ID20854371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61647701..61655100hg38UCSC Ensembl
chr1:62113373..62120772hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv207n223
Supporting Variantsnssv18062151
Samples
Known GenesMGC34796
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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