A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330457



Internal ID20863614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5563801..5564800hg38UCSC Ensembl
chr1:5623861..5624860hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061660
Samples
Known GenesMIR4417
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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