A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439347



Internal ID22497217
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 StatusS
Merged Variantsnsv5877440
Supporting Variants
Samples
Known GenesFIGF, PIR-FIGF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439347
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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