A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551135



Internal ID20885864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70702210..70702871hg38UCSC Ensembl
chr2:70929342..70930003hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258944
Samples
Known GenesADD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551135
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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