A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3786



Internal ID15538513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49590227..49591348hg38UCSC Ensembl
OuterchrX:49354830..49355951hg19UCSC Ensembl
OuterchrX:49241774..49242895hg18UCSC Ensembl
OuterchrX:49058041..49059162hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3824098
hg1924098
hg1824098
hg1724098
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6899
Supporting Variants
SamplesNA12878
Known GenesGAGE2A
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)nssv3786
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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