A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587316



Internal ID20960387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43819542..43820174hg38UCSC Ensembl
chr15:44111740..44112372hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2514n223
Supporting Variantsnssv18239576
Samples
Known GenesMFAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587316
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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