A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742530



Internal ID20518514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140035865..140035923hg38UCSC Ensembl
chr7:139735665..139735723hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295156
Samples
Known GenesPARP12
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742530
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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