A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7026



Internal ID15551994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:107044756..107090097hg38UCSC Ensembl
OuterchrX:106287986..106333327hg19UCSC Ensembl
OuterchrX:106174642..106219983hg18UCSC Ensembl
OuterchrX:106094131..106139472hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3845342
hg1945342
hg1845342
hg1745342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6361
SamplesNA12156
Known GenesRBM41
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)nsv7026
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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