A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8762



Internal ID15535102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:110241474..110286240hg38UCSC Ensembl
OuterchrX:109484702..109529468hg19UCSC Ensembl
OuterchrX:109371358..109416124hg18UCSC Ensembl
OuterchrX:109290847..109335613hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3844767
hg1944767
hg1844767
hg1744767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7036
Supporting Variants
SamplesNA12156
Known GenesAMMECR1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv8762
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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