A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552751



Internal ID20925877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61365316..61365977hg38UCSC Ensembl
chr2:61592451..61593112hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258308
Samples
Known GenesUSP34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552751
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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