A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004881



Internal ID17297833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:150718951..150719311hg38UCSC Ensembl
Outerchr1:150691427..150691787hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958528
Supporting Variants
SamplesBILGI_BIOE
Known GenesHORMAD1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004881
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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