A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527347



Internal ID15107954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:114537428..114983201hg38UCSC Ensembl
InnerchrX:113771881..114217764hg19UCSC Ensembl
InnerchrX:113678137..114124020hg18UCSC Ensembl
InnerchrX:113594861..114040744hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38445774
hg19445884
hg18445884
hg17445884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703774
Samples
Known GenesHTR2C, MIR1264, MIR1298, MIR1911, MIR1912, MIR448, MIR764, SNORA35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527347
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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