A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602720



Internal ID20975791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18807772..18808563hg38UCSC Ensembl
chr7:18847395..18848186hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156675
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602720
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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