A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654146



Internal ID15390798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:118534120..118830196hg38UCSC Ensembl
InnerchrX:117668083..117964159hg19UCSC Ensembl
InnerchrX:117552111..117848187hg18UCSC Ensembl
InnerchrX:117449965..117746041hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38296077
hg19296077
hg18296077
hg17296077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517257
Supporting Variants
Samples
Known GenesDOCK11, IL13RA1, ZCCHC12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654146
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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