A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9929



Internal ID15540015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150062387..150081542hg38UCSC Ensembl
OuterchrX:149230618..149249773hg19UCSC Ensembl
OuterchrX:148981276..149000431hg18UCSC Ensembl
OuterchrX:148901186..148920341hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3819156
hg1919156
hg1819156
hg1719156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7148
Supporting Variants
SamplesNA18507
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)nssv9929
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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