A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076444



Internal ID21985677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82140599..82140599hg38UCSC Ensembl
chr5:81436418..81436418hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549590
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076444
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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