A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433162



Internal ID21395164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70308759..70309715hg38UCSC Ensembl
chr1:70774442..70775398hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750257
SamplesMDQ025
Known GenesANKRD13C
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433162
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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