A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557634



Internal ID20930705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79121537..79122000hg38UCSC Ensembl
chr5:78417360..78417823hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270285
Samples
Known GenesBHMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557634
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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