A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9932



Internal ID15540019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:12358236..12385372hg38UCSC Ensembl
OuterchrY:14478967..14497167hg19UCSC Ensembl
OuterchrY:12988975..13007175hg18UCSC Ensembl
OuterchrY:12917712..12935912hg17UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3810160
hg1910160
hg1810160
hg1710160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7170
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)nssv9932
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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