A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356897



Internal ID21014450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113940995..113945561hg38UCSC Ensembl
chr3:113659842..113664408hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg384567
hg194567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093168
Samples
Known GenesGRAMD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer