A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657262



Internal ID21605567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9955567..9955567hg38UCSC Ensembl
chr17:9858884..9858884hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099896
SamplesHG01505
Known GenesGAS7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657262
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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