A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15196748



Internal ID21335544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150084360..150084467hg38UCSC Ensembl
chr5:149463923..149464030hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939882
Supporting Variants
SamplesHG002
Known GenesCSF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15196748
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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