A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577224



Internal ID21525673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210111289..210116040hg38UCSC Ensembl
chr1:210284634..210289385hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg384752
hg194752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062643
SamplesHG02587
Known GenesSYT14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577224
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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