A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605889



Internal ID20978960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116894801..116896700hg38UCSC Ensembl
chr7:116534855..116536754hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148602
Samples
Known GenesCAPZA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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