A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10506



Internal ID15542292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:76377300..76398167hg38UCSC Ensembl
Outerchr6:77087017..77107884hg19UCSC Ensembl
Outerchr6:77143737..77164604hg18UCSC Ensembl
Outerchr6:77143737..77164604hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3820868
hg1920868
hg1820868
hg1720868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5358
Supporting Variants
SamplesNA18956
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)nssv10506
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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