A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370977



Internal ID21028530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151005747..151008929hg38UCSC Ensembl
chr3:150723534..150726716hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg383183
hg193183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096593
Samples
Known GenesCLRN1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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