A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154338



Internal ID21425203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76699599..76699794hg38UCSC Ensembl
chr5:75995424..75995619hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569855
Supporting Variants
SamplesHG00731
Known GenesIQGAP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154338
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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