A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4907



Internal ID15549663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:84640927..84668426hg38UCSC Ensembl
Outerchr5:83936745..83964244hg19UCSC Ensembl
Outerchr5:83972501..84000000hg18UCSC Ensembl
Outerchr5:83972501..84000000hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3827500
hg1927500
hg1827500
hg1727500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6010, nssv3365, nssv2529, nssv4849
SamplesNA12156, NA12878, NA18555, NA19129
Known Genes
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)nsv4907
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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