A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605023



Internal ID20978094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2413874..2414354hg38UCSC Ensembl
chr7:2453509..2453989hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154980
Samples
Known GenesCHST12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605023
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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