A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614584



Internal ID20987655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2938887..3089325hg38UCSC Ensembl
chr7:2978521..3128959hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38150439
hg19150439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155643
Samples
Known GenesCARD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614584
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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