A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2977656



Internal ID15593042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:101801475..101830891hg38UCSC Ensembl
InnerchrX:101056448..101085864hg19UCSC Ensembl
InnerchrX:100943104..100972520hg18UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3829417
hg1929417
hg1829417
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515160
Supporting Variants
SamplesNA07037
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2977656
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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