A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735004



Internal ID20510944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122705700..122705962hg38UCSC Ensembl
chr7:122345754..122346016hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277211
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735004
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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