A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609479



Internal ID20982550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38985963..38986593hg38UCSC Ensembl
chr7:39025563..39026193hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156557
Samples
Known GenesPOU6F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609479
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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