A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7087



Internal ID15205375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:129815037..129860444hg38UCSC Ensembl
OuterchrX:128949013..128994420hg19UCSC Ensembl
OuterchrX:128776694..128822101hg18UCSC Ensembl
OuterchrX:128674548..128719955hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3845408
hg1945408
hg1845408
hg1745408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6373
SamplesNA12156
Known GenesZDHHC9
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)nsv7087
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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