A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4919



Internal ID15549676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:94325874..94345694hg38UCSC Ensembl
Outerchr5:93661579..93681399hg19UCSC Ensembl
Outerchr5:93687335..93707155hg18UCSC Ensembl
Outerchr5:93687335..93707155hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3819821
hg1919821
hg1819821
hg1719821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8122
SamplesNA12156
Known GenesKIAA0825
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)nsv4919
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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