A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575946



Internal ID21524380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107053172..107053328hg38UCSC Ensembl
chr4:107974329..107974485hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138276
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575946
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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