A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522012



Internal ID15449305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:10487245..10567798hg38UCSC Ensembl
InnerchrX:10455285..10535838hg19UCSC Ensembl
InnerchrX:10415285..10495838hg18UCSC Ensembl
InnerchrX:10265021..10345574hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3880554
hg1980554
hg1880554
hg1780554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv500n21
Supporting Variantsnssv694781
Samples
Known GenesMID1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522012
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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