A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537511



Internal ID20910845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9753494..9754653hg38UCSC Ensembl
chr1:9813552..9814711hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381160
hg191160
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252786
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537511
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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