A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555725



Internal ID20928796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25140746..25141476hg38UCSC Ensembl
chr7:25180365..25181095hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273340
Samples
Known GenesC7orf31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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