A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618562



Internal ID20991633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95267001..95268200hg38UCSC Ensembl
chr7:94896313..94897512hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161616
Samples
Known GenesPPP1R9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618562
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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