A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1672321



Internal ID15183143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135287530..135464387hg38UCSC Ensembl
InnerchrX:134421462..134598312hg19UCSC Ensembl
InnerchrX:134249128..134425978hg18UCSC Ensembl
InnerchrX:133127069..133303919hg16UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38176858
hg19176851
hg18176851
hg16176851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469871
Supporting Variants
Samples
Known GenesLINC00086, LOC100506790, ZNF449, ZNF75D
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nssv1672321
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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