A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10750



Internal ID15542048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155545842..155579416hg38UCSC Ensembl
OuterchrX:154775503..154809077hg19UCSC Ensembl
OuterchrX:154428697..154462271hg18UCSC Ensembl
OuterchrX:154339207..154372781hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3833575
hg1933575
hg1833575
hg1733575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7162
Supporting Variants
SamplesNA18956
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)nssv10750
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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