A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8806



Internal ID15188372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150793611..150830627hg38UCSC Ensembl
OuterchrX:149962084..149999100hg19UCSC Ensembl
OuterchrX:149712742..149749758hg18UCSC Ensembl
OuterchrX:149632652..149669668hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3837017
hg1937017
hg1837017
hg1737017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7151
Supporting Variants
SamplesNA12156
Known GenesCD99L2
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)nssv8806
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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