A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7068



Internal ID15552040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:123551444..123597117hg38UCSC Ensembl
OuterchrX:122685295..122730968hg19UCSC Ensembl
OuterchrX:122512976..122558649hg18UCSC Ensembl
OuterchrX:122410830..122456503hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3845674
hg1945674
hg1845674
hg1745674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6370
SamplesNA12156
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)nsv7068
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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