A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007069



Internal ID22068700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:19035841..19044494hg38UCSC Ensembl
Outerchr1:19033451..19045592hg38UCSC Ensembl
Innerchr1:19362335..19370988hg19UCSC Ensembl
Outerchr1:19359945..19372086hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3812142
hg1912142
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154670
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007069
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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