A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732244



Internal ID20508168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38878508..38878597hg38UCSC Ensembl
chr1:39344180..39344269hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270007
Samples
Known GenesGJA9, GJA9-MYCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732244
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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