A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527976



Internal ID15455269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:34926881..35564261hg38UCSC Ensembl
InnerchrX:34944998..35582378hg19UCSC Ensembl
InnerchrX:34854919..35492299hg18UCSC Ensembl
InnerchrX:34704655..35342035hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38637381
hg19637381
hg18637381
hg17637381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704491
Samples
Known GenesFAM47B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527976
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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