A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177705



Internal ID21316501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113130556..113130728hg38UCSC Ensembl
chr2:113888133..113888305hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938873
Supporting Variants
SamplesHG002
Known GenesIL1RN
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177705
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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