A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526896



Internal ID15107503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:150473747..150475142hg38UCSC Ensembl
InnerchrX:149642019..149643414hg19UCSC Ensembl
InnerchrX:149392677..149394072hg18UCSC Ensembl
InnerchrX:149312587..149313982hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381396
hg191396
hg181396
hg171396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703254
Samples
Known GenesMAMLD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526896
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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