A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577120



Internal ID21525567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61274127..61274261hg38UCSC Ensembl
chr2:61501262..61501396hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114616
SamplesNA18939
Known GenesUSP34
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577120
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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