A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684177



Internal ID15074143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:41140431..41257277hg38UCSC Ensembl
InnerchrX:40999684..41116530hg19UCSC Ensembl
InnerchrX:40884628..41001474hg18UCSC Ensembl
InnerchrX:40755938..40872784hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38116847
hg19116847
hg18116847
hg17116847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516661
Supporting Variants
Samples
Known GenesUSP9X
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684177
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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