A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607213



Internal ID20980284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97701701..97704300hg38UCSC Ensembl
chr7:97331013..97333612hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607213
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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