A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901207



Internal ID22676355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5862257..5862343hg38UCSC Ensembl
chr4:5863984..5864070hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418888
Samples
Known GenesCRMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901207
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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