A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606263



Internal ID20979334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121840331..121872576hg38UCSC Ensembl
chr7:121480385..121512630hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3832246
hg1932246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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