A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6915



Internal ID15205186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55931790..55963165hg38UCSC Ensembl
OuterchrX:55958223..55989598hg19UCSC Ensembl
OuterchrX:55974948..56006323hg18UCSC Ensembl
OuterchrX:55841244..55872619hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg388118
hg198118
hg188118
hg178118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10715
SamplesNA18956
Known Genes
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)nsv6915
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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