A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606547



Internal ID20979618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107621827..107641838hg38UCSC Ensembl
chr7:107262272..107282283hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3820012
hg1920012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146982
Samples
Known GenesBCAP29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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