A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7162



Internal ID15205458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155545842..155591711hg38UCSC Ensembl
OuterchrX:154775503..154821372hg19UCSC Ensembl
OuterchrX:154428697..154474566hg18UCSC Ensembl
OuterchrX:154339207..154385076hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3845870
hg1945870
hg1845870
hg1745870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10750, nssv5277, nssv1885, nssv3835, nssv6391
SamplesNA18956, NA19129, NA12156, NA12878, NA18555
Known GenesTMLHE
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)nsv7162
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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