A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597801



Internal ID21546420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38099928..38100996hg38UCSC Ensembl
chr10:38388856..38389924hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070199
SamplesHG03683
Known GenesZNF37A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597801
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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