A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7016



Internal ID15205297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:101988705..102021775hg38UCSC Ensembl
OuterchrX:101243678..101276748hg19UCSC Ensembl
OuterchrX:101130334..101163404hg18UCSC Ensembl
OuterchrX:101049823..101082893hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg386368
hg196368
hg186368
hg176368
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8758
SamplesNA12156
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)nsv7016
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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