A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575598



Internal ID20948669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90643181..90643752hg38UCSC Ensembl
chr14:91109525..91110096hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2235n223
Supporting Variantsnssv18237651
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575598
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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