A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7019



Internal ID15551986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:104376282..104409571hg38UCSC Ensembl
OuterchrX:103620963..103654252hg19UCSC Ensembl
OuterchrX:103507619..103540908hg18UCSC Ensembl
OuterchrX:103427108..103460397hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg387694
hg197694
hg187694
hg177694
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv897
SamplesNA19240
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)nsv7019
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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