A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7150



Internal ID15205445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150773003..150802297hg38UCSC Ensembl
OuterchrX:149941476..149970770hg19UCSC Ensembl
OuterchrX:149692134..149721428hg18UCSC Ensembl
OuterchrX:149612044..149641338hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3810734
hg1910734
hg1810734
hg1710734
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1880
SamplesNA18555
Known GenesCD99L2
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)nsv7150
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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