A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7018



Internal ID15551985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:103882321..103911332hg38UCSC Ensembl
OuterchrX:103137225..103166252hg19UCSC Ensembl
OuterchrX:103023881..103052908hg18UCSC Ensembl
OuterchrX:102943370..102972397hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3829012
hg1929028
hg1829028
hg1729028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3815, nssv6358
SamplesNA12156, NA12878
Known GenesMIR1256
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)nsv7018
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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