A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9477



Internal ID15540191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9401474..9406955hg38UCSC Ensembl
OuterchrX:9369514..9374995hg19UCSC Ensembl
OuterchrX:9329514..9334995hg18UCSC Ensembl
OuterchrX:9179250..9184731hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3822502
hg1922502
hg1822502
hg1722502
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6792
Supporting Variants
SamplesNA18517
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)nssv9477
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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