A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070180



Internal ID21441032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35150828..35150892hg38UCSC Ensembl
chr10:35439756..35439820hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590032
Supporting Variants
SamplesHG00732
Known GenesCREM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070180
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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