A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6872



Internal ID15551825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:40855512..40894200hg38UCSC Ensembl
OuterchrX:40714765..40753453hg19UCSC Ensembl
OuterchrX:40599709..40638397hg18UCSC Ensembl
OuterchrX:40471019..40509707hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg385590
hg195590
hg185590
hg175590
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5211, nssv8711
SamplesNA12156, NA19129
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)nsv6872
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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