A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6328



Internal ID15190850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49318285..49327273hg38UCSC Ensembl
OuterchrX:49174764..49183733hg19UCSC Ensembl
OuterchrX:49061708..49070677hg18UCSC Ensembl
OuterchrX:48931135..48940104hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3818044
hg1918044
hg1818044
hg1718044
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6896
Supporting Variants
SamplesNA12156
Known GenesGAGE10, GAGE12J
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)nssv6328
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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