A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438155



Internal ID15387966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:123971941..123972647hg38UCSC Ensembl
InnerchrX:123105791..123106497hg19UCSC Ensembl
InnerchrX:122933472..122934178hg18UCSC Ensembl
InnerchrX:121803546..121804252hg16UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38707
hg19707
hg18707
hg16707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470221, nssv470222
SamplesNA18995, NA18540
Known GenesSTAG2
MethodSNP array
AnalysisNull genotypes - for each genotype assay and population sample we defined the null genotype pattern of that assay as the binary vector (length 90) of null genotype calls across the 90 individuals.
PlatformNot reported
Comments
ReferenceMcCarroll_et_al_2006
Pubmed ID16468122
Accession Number(s)nsv438155
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer