A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394014



Internal ID21051567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39557433..39558157hg38UCSC Ensembl
chr4:39559053..39559777hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116100
Samples
Known GenesMIR1273H, SMIM14, UGDH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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