A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942870



Internal ID21362939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72064898..72065202hg38UCSC Ensembl
chr10:73824656..73824960hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181534
SamplesHG002
Known GenesSPOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942870
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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