A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739060



Internal ID20515032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56041383..56041459hg38UCSC Ensembl
chr7:56109076..56109152hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262243
Samples
Known GenesPSPH
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739060
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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