A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6896



Internal ID15205165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49318285..49327859hg38UCSC Ensembl
OuterchrX:49174764..49184319hg19UCSC Ensembl
OuterchrX:49061708..49071263hg18UCSC Ensembl
OuterchrX:48931135..48940690hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3818044
hg1918044
hg1818044
hg1718044
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv867, nssv9482, nssv10705, nssv866, nssv6328, nssv5222
SamplesNA12156, NA18956, NA18517, NA19240, NA19129
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)nsv6896
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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