A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385472



Internal ID21043025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153306401..153309500hg38UCSC Ensembl
chr4:154227553..154230652hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110890
Samples
Known GenesANXA2P1, TRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385472
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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