A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411200



Internal ID21068753
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 StatusM
Merged Variants
Supporting Variantsnssv18145848
Samples
Known GenesBMP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411200
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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