A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521021



Internal ID15448314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:139560234..139566367hg38UCSC Ensembl
InnerchrX:138642393..138648526hg19UCSC Ensembl
InnerchrX:138470059..138476192hg18UCSC Ensembl
InnerchrX:138367913..138374046hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg386134
hg196134
hg186134
hg176134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679989, nssv688511, nssv685013
Samples
Known GenesF9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521021
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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