A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608152



Internal ID20981223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37898020..37898421hg38UCSC Ensembl
chr7:37937622..37938023hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156455
Samples
Known GenesNME8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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