A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751137



Internal ID20526997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27613122..27613122hg38UCSC Ensembl
chr7:27652741..27652741hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269578
Samples
Known GenesHIBADH
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751137
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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