A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6816



Internal ID15205077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:16650590..16681559hg38UCSC Ensembl
OuterchrX:16668713..16699682hg19UCSC Ensembl
OuterchrX:16578634..16609603hg18UCSC Ensembl
OuterchrX:16428370..16459339hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3810024
hg1910024
hg1810024
hg1710024
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv853
SamplesNA19240
Known GenesCTPS2, S100G
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)nsv6816
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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