A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877440



Internal ID22652405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15370412..15377397hg38UCSC Ensembl
chrX:15388534..15395519hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg386986
hg196986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439347
Samples
Known GenesFIGF, PIR-FIGF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877440
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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