A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370768



Internal ID21028321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101300152..101300666hg38UCSC Ensembl
chr3:101018996..101019510hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092381
Samples
Known GenesIMPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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