A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608845



Internal ID20981916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24670331..24670732hg38UCSC Ensembl
chr7:24709950..24710351hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155027
Samples
Known GenesMPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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