A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535701



Internal ID20909055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237503557..237510428hg38UCSC Ensembl
chr2:238412200..238419071hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg386872
hg196872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257417
Samples
Known GenesMLPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535701
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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