A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877



Internal ID15198375
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 StatusS
Merged Variantsnsv6919
Supporting Variants
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)nssv877
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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