A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390275



Internal ID21047828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53049111..53049527hg38UCSC Ensembl
chr4:53915278..53915694hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117383
Samples
Known GenesSCFD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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