A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584095



Internal ID21532629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43128820..43128964hg38UCSC Ensembl
chr7:43168419..43168563hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158514
SamplesHG00171
Known GenesHECW1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584095
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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