A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700054



Internal ID15090020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155670185..155699751hg38UCSC Ensembl
InnerchrX:154899846..154929412hg19UCSC Ensembl
InnerchrX:154553040..154582606hg18UCSC Ensembl
InnerchrX:154463550..154493116hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3829567
hg1929567
hg1829567
hg1729567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520699
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700054
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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