A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7073



Internal ID15552046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:125145307..125153814hg38UCSC Ensembl
OuterchrX:124279156..124287663hg19UCSC Ensembl
OuterchrX:124106837..124115344hg18UCSC Ensembl
OuterchrX:124004691..124013198hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg388508
hg198508
hg188508
hg178508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8776
SamplesNA12156
Known Genes
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)nsv7073
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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