A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425276



Internal ID21082829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130576053..130598476hg38UCSC Ensembl
chr7:130260325..130283354hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3822424
hg1923030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153447
Samples
Known GenesCOPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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