A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602182



Internal ID20975253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74630155..74631054hg38UCSC Ensembl
chr7:74044471..74045370hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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