A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2977995



Internal ID15655753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:117626457..117850009hg38UCSC Ensembl
InnerchrX:116760420..116983972hg19UCSC Ensembl
InnerchrX:116644448..116868000hg18UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38223553
hg19223553
hg18223553
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515164
Supporting Variants
SamplesNA12864
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2977995
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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