A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6919



Internal ID15205190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:57569392..57601519hg38UCSC Ensembl
OuterchrX:57595825..57627952hg19UCSC Ensembl
OuterchrX:57612550..57644677hg18UCSC Ensembl
OuterchrX:57478846..57510973hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg388866
hg198866
hg188866
hg178866
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877
SamplesNA19240
Known GenesZXDB
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)nsv6919
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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