A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521599



Internal ID15102206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:78406942..78868581hg38UCSC Ensembl
InnerchrX:77662439..78124078hg19UCSC Ensembl
InnerchrX:77549095..78010734hg18UCSC Ensembl
InnerchrX:77468584..77930223hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38461640
hg19461640
hg18461640
hg17461640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv517n21
Supporting Variantsnssv698216
Samples
Known GenesLPAR4, ZCCHC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521599
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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