A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604825



Internal ID20977896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35966801..35977600hg38UCSC Ensembl
chr7:36006411..36017210hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3810800
hg1910800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604825
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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