A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356113



Internal ID21013666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127611674..127612000hg38UCSC Ensembl
chr3:127330517..127330843hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094106
Samples
Known GenesMCM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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