A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557004



Internal ID20930075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31943968..32642088hg38UCSC Ensembl
chr5:31944074..32642194hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38698121
hg19698121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268165
Samples
Known GenesGOLPH3, MTMR12, PDZD2, SUB1, ZFR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557004
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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