A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556



Internal ID15550377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:156939822..156985174hg38UCSC Ensembl
Outerchr6:157260956..157306308hg19UCSC Ensembl
Outerchr6:157302648..157348000hg18UCSC Ensembl
Outerchr6:157353069..157398421hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3845353
hg1945353
hg1845353
hg1745353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6100
SamplesNA12156
Known GenesARID1B
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)nsv5556
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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