A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602128



Internal ID20975199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111722113..111735356hg38UCSC Ensembl
chr7:111362169..111375412hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3813244
hg1913244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149517
Samples
Known GenesDOCK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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