A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564866



Internal ID20937937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137065219..137066344hg38UCSC Ensembl
chr5:136400908..136402033hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267390
Samples
Known GenesSPOCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564866
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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