A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616118



Internal ID20989189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92626889..92627430hg38UCSC Ensembl
chr7:92256203..92256744hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159997
Samples
Known GenesCDK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616118
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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