A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145848



Internal ID20712888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55843937..55844468hg38UCSC Ensembl
chr6:55708735..55709266hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411200
Supporting Variants
Samples
Known GenesBMP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00101


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