A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000507



Internal ID16946773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:216011983..216012144hg38UCSC Ensembl
Outerchr1:216185325..216185486hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954217
Supporting Variants
SamplesBILGI_BIOE
Known GenesUSH2A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000507
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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