A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322436



Internal ID20855549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241085498..241091555hg38UCSC Ensembl
chr1:241248798..241254855hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg386058
hg196058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059060
Samples
Known GenesRGS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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