A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv821416



Internal ID6111063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16171777..16173975hg19UCSC Ensembl
Innerchr7:16138302..16140500hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1420644
SamplesNA10851
Known GenesISPD
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformIllumina IIx
Comments
ReferenceJu_et_al_2010
Pubmed ID20802225
Accession Number(s)nsv821416
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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