A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197705



Internal ID21336501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119096338..119096666hg38UCSC Ensembl
chr6:119417503..119417831hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925049
Supporting Variants
SamplesHG002
Known GenesFAM184A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197705
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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