A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6125



Internal ID15204317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:25410366..25444678hg38UCSC Ensembl
Outerchr8:25267882..25302194hg19UCSC Ensembl
Outerchr8:25323799..25358111hg18UCSC Ensembl
Outerchr8:25323799..25358111hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg386664
hg196664
hg186664
hg176664
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv724
SamplesNA19240
Known GenesDOCK5, GNRH1, KCTD9
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)nsv6125
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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