A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178995



Internal ID21317791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55720145..55720208hg38UCSC Ensembl
chr3:55754173..55754236hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951578
Supporting Variants
SamplesHG002
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178995
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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