A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537676



Internal ID20911011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233138201..233138983hg38UCSC Ensembl
chr2:234002911..234003693hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257369
Samples
Known GenesINPP5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537676
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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