A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7152



Internal ID15552133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151157229..151201873hg38UCSC Ensembl
OuterchrX:150325701..150370345hg19UCSC Ensembl
OuterchrX:150076359..150121003hg18UCSC Ensembl
OuterchrX:149996269..150040913hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3844645
hg1944645
hg1844645
hg1744645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8807
SamplesNA12156
Known GenesGPR50, MIR4330
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)nsv7152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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