A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021028



Internal ID22082659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:150700888..150703805hg38UCSC Ensembl
Outerchr1:150698922..150704541hg38UCSC Ensembl
Innerchr1:150673364..150676281hg19UCSC Ensembl
Outerchr1:150671398..150677017hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg385620
hg195620
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156614
Supporting Variants
Samples
Known GenesHORMAD1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021028
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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