A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412607



Internal ID21070160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1529611..1533327hg38UCSC Ensembl
chr6:1529846..1533562hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg383717
hg193717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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