A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574592



Internal ID20947663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5998081..5998652hg38UCSC Ensembl
chr7:6037712..6038283hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6554n223
Supporting Variantsnssv18275431
Samples
Known GenesPMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574592
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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