A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434803



Internal ID21396805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159665254..159667646hg38UCSC Ensembl
chr6:160086286..160088678hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382393
hg192393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv725n172
Supporting Variantsnssv15752077, nssv15751049, nssv15749891, nssv15750537, nssv15752329
SamplesBTQ055, SMI041, NB07, MDQ025, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434803
Frequency
Sample Size15
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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