A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7159



Internal ID15205454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:153817798..153863078hg38UCSC Ensembl
OuterchrX:153083253..153128533hg19UCSC Ensembl
OuterchrX:152736447..152781727hg18UCSC Ensembl
OuterchrX:152604100..152649380hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3845281
hg1945281
hg1845281
hg1745281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8809
SamplesNA12156
Known GenesL1CAM, PDZD4
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)nsv7159
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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