A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694576



Internal ID15084542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:154802735..154831402hg38UCSC Ensembl
InnerchrX:154031010..154059677hg19UCSC Ensembl
InnerchrX:153684204..153712871hg18UCSC Ensembl
InnerchrX:153594714..153623381hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3828668
hg1928668
hg1828668
hg1728668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516158
Supporting Variants
Samples
Known GenesMPP1, SMIM9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694576
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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