A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738200



Internal ID20514167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119755900..119756377hg38UCSC Ensembl
chr10:121515412..121515889hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280008
Samples
Known GenesINPP5F
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738200
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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