A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2752



Internal ID15200629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:63536774..63569950hg38UCSC Ensembl
Outerchr2:63763908..63797084hg19UCSC Ensembl
Outerchr2:63617412..63650588hg18UCSC Ensembl
Outerchr2:63675559..63708735hg17UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg386574
hg196574
hg186574
hg176574
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4421
SamplesNA12878
Known GenesWDPCP
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)nsv2752
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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