A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537296



Internal ID20910634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38880014..38880174hg38UCSC Ensembl
chr1:39345686..39345846hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252420
Samples
Known GenesGJA9, GJA9-MYCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537296
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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