A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604620



Internal ID20977691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23496556..23536939hg38UCSC Ensembl
chr7:23536175..23576558hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3840384
hg1940384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154927
Samples
Known GenesTRA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604620
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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