A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557



Internal ID15551478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:70861662..70895864hg38UCSC Ensembl
Outerchr9:73476578..73510780hg19UCSC Ensembl
Outerchr9:72666398..72700600hg18UCSC Ensembl
Outerchr9:70706132..70740334hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385785
hg195785
hg185785
hg175785
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2812
SamplesNA18555
Known GenesTRPM3
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)nsv6557
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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