A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525246



Internal ID15452539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:127603746..127625238hg38UCSC Ensembl
InnerchrX:126737727..126759219hg19UCSC Ensembl
InnerchrX:126565408..126586900hg18UCSC Ensembl
InnerchrX:126463262..126484754hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3821493
hg1921493
hg1821493
hg1721493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701337
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525246
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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