A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434802



Internal ID21396804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159665196..159667646hg38UCSC Ensembl
chr6:160086228..160088678hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382451
hg192451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv725n172
Supporting Variantsnssv15749157
SamplesNB11
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434802
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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