A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518527



Internal ID15445820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:127737006..127885040hg38UCSC Ensembl
InnerchrX:126870987..127019019hg19UCSC Ensembl
InnerchrX:126698668..126846700hg18UCSC Ensembl
InnerchrX:126596522..126744554hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38148035
hg19148033
hg18148033
hg17148033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695970
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518527
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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