A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407949



Internal ID21065502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160644209..160664554hg38UCSC Ensembl
chr5:160071216..160091561hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3820346
hg1920346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127519
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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