A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747102



Internal ID20523119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64426697..64426891hg38UCSC Ensembl
chr12:64820477..64820671hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272505
Samples
Known GenesXPOT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747102
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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