A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2410



Internal ID15194038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:123866018..123898685hg38UCSC Ensembl
Outerchr3:123584865..123617532hg19UCSC Ensembl
Outerchr3:125067555..125100222hg18UCSC Ensembl
Outerchr3:125067555..125100222hg17UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg386963
hg196963
hg186963
hg176963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3979
Supporting Variants
SamplesNA18555
Known GenesMYLK
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)nssv2410
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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