A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368434



Internal ID21025987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151199974..151200593hg38UCSC Ensembl
chr3:150917761..150918380hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096601
Samples
Known GenesGPR171, MED12L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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