A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1820



Internal ID15541103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:5035179..5065049hg38UCSC Ensembl
OuterchrX:4953220..4983090hg19UCSC Ensembl
OuterchrX:4963220..4993090hg18UCSC Ensembl
OuterchrX:4812956..4842826hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3810160
hg1910160
hg1810160
hg1710160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6782
Supporting Variants
SamplesNA18555
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)nssv1820
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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