A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3787



Internal ID15538514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49603030..49612677hg38UCSC Ensembl
OuterchrX:49367633..49377280hg19UCSC Ensembl
OuterchrX:49254577..49264232hg18UCSC Ensembl
OuterchrX:49070873..49080528hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3828432
hg1928432
hg1828432
hg1728432
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6899
Supporting Variants
SamplesNA12878
Known GenesGAGE1
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)nssv3787
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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