A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327986



Internal ID20861130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238320526..238323327hg38UCSC Ensembl
chr1:238483826..238486627hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv565n223
Supporting Variantsnssv18059284
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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