A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527628



Internal ID15454921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:150530767..150558638hg38UCSC Ensembl
InnerchrX:149699221..149727091hg19UCSC Ensembl
InnerchrX:149449879..149477749hg18UCSC Ensembl
InnerchrX:149369789..149397659hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3827872
hg1927871
hg1827871
hg1727871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704096
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527628
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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