A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704650



Internal ID15441302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29071792..29133087hg38UCSC Ensembl
InnerchrX:29089909..29151204hg19UCSC Ensembl
InnerchrX:28999830..29061125hg18UCSC Ensembl
InnerchrX:28849566..28910861hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3861296
hg1961296
hg1861296
hg1761296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516364
Supporting Variants
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704650
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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