A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6927



Internal ID15551885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:63975515..64009961hg38UCSC Ensembl
OuterchrX:63195395..63229841hg19UCSC Ensembl
OuterchrX:63112120..63146566hg18UCSC Ensembl
OuterchrX:62978416..63012862hg17UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg385574
hg195574
hg185574
hg175574
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2832
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)nsv6927
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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