A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177999



Internal ID21316795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214864037..214866107hg38UCSC Ensembl
chr2:215728761..215730831hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382071
hg192071
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934500
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177999
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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