A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431150



Internal ID21393152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106190927..106191837hg38UCSC Ensembl
chr10:107950685..107951595hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv94n172
Supporting Variantsnssv15749849, nssv15750857, nssv15751450, nssv15752524, nssv15752015, nssv15746502, nssv15754619, nssv15751942, nssv15752280, nssv15746896, nssv15745832, nssv15753789, nssv15750722
SamplesNB12, SMI034, NB08, BTQ038, NB10, BTQ055, MDQ010, BTQ016, SMI041, NB11, NB07, SMI018, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431150
Frequency
Sample Size15
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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