A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7064



Internal ID15552036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:122265349..122291373hg38UCSC Ensembl
OuterchrX:121399202..121425226hg19UCSC Ensembl
OuterchrX:121226883..121252907hg18UCSC Ensembl
OuterchrX:121124737..121150761hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3826025
hg1926025
hg1826025
hg1726025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8772
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)nsv7064
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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