A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377544



Internal ID21035097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:115008396..115387707hg38UCSC Ensembl
chr4:115929552..116308863hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38379312
hg19379312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105820
Samples
Known GenesNDST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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