A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2837



Internal ID15200714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:97694463..97728803hg38UCSC Ensembl
Outerchr2:98310926..98345266hg19UCSC Ensembl
Outerchr2:97677358..97711698hg18UCSC Ensembl
Outerchr2:97769444..97803784hg17UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg385400
hg195400
hg185400
hg175400
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4441
SamplesNA12878
Known GenesLINC01125, ZAP70
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)nsv2837
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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