A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763



Internal ID15538491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:5039776..5051961hg38UCSC Ensembl
OuterchrX:4957817..4970002hg19UCSC Ensembl
OuterchrX:4967817..4980002hg18UCSC Ensembl
OuterchrX:4817553..4829738hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg389635
hg199635
hg189635
hg179635
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6782
Supporting Variants
SamplesNA12878
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)nssv3763
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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