A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527818



Internal ID20901179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1392130..1392558hg38UCSC Ensembl
chr19:1392129..1392557hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045885
Samples
Known GenesNDUFS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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