A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545099



Internal ID20918330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38924901..38925023hg38UCSC Ensembl
chr1:39390573..39390695hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252423
Samples
Known GenesRHBDL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545099
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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