A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700470



Internal ID15437122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:143332263..143402732hg38UCSC Ensembl
InnerchrX:142420057..142490526hg19UCSC Ensembl
InnerchrX:142247723..142318192hg18UCSC Ensembl
InnerchrX:142145577..142216046hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3870470
hg1970470
hg1870470
hg1770470
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524522
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700470
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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