A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571854



Internal ID20944925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44751675..44752379hg38UCSC Ensembl
chr7:44791274..44791978hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275999
Samples
Known GenesZMIZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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