A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734695



Internal ID20510633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35576936..35576988hg38UCSC Ensembl
chr1:36042537..36042589hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270272
Samples
Known GenesTFAP2E
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734695
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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