A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438138



Internal ID15387949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:76909582..76923979hg38UCSC Ensembl
InnerchrX:76130008..76144404hg19UCSC Ensembl
InnerchrX:76046402..76060798hg18UCSC Ensembl
InnerchrX:74996468..75010864hg16UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3814398
hg1914397
hg1814397
hg1614397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470176
SamplesNA12864
Known GenesMIR384
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)nsv438138
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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