A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432152



Internal ID21089705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148475746..148476626hg38UCSC Ensembl
chr7:148172838..148173718hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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