A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552309



Internal ID20925436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173754412..173755083hg38UCSC Ensembl
chr1:173723551..173724222hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248116
Samples
Known GenesKLHL20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552309
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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