A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6852



Internal ID15551803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:33398674..33413943hg38UCSC Ensembl
OuterchrX:33416791..33432060hg19UCSC Ensembl
OuterchrX:33326712..33341981hg18UCSC Ensembl
OuterchrX:33176448..33191717hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg386009
hg196009
hg186009
hg176009
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2828
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)nsv6852
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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