A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329014



Internal ID20862165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70818892..70819515hg38UCSC Ensembl
chr1:71284575..71285198hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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