A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526948



Internal ID15107555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:27464175..27901289hg38UCSC Ensembl
InnerchrX:27482292..27919406hg19UCSC Ensembl
InnerchrX:27392213..27829327hg18UCSC Ensembl
InnerchrX:27241949..27679063hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38437115
hg19437115
hg18437115
hg17437115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703318
Samples
Known GenesDCAF8L2, MAGEB10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526948
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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