A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544837



Internal ID20918074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236571069..236571203hg38UCSC Ensembl
chr2:237479712..237479846hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257410
Samples
Known GenesACKR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544837
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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