A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755177



Internal ID20531037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73578765..73578765hg38UCSC Ensembl
chr7:72993095..72993095hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755177
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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