A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15183983



Internal ID21322779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90630742..90631075hg38UCSC Ensembl
chr15:91173974..91174307hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948011
Supporting Variants
SamplesHG002
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15183983
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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