A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7078



Internal ID15205365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:126537222..126569770hg38UCSC Ensembl
OuterchrX:125671205..125703753hg19UCSC Ensembl
OuterchrX:125498886..125531434hg18UCSC Ensembl
OuterchrX:125396740..125429288hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg386960
hg196960
hg186960
hg176960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10735
SamplesNA18956
Known GenesDCAF12L1
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)nsv7078
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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