A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17396102



Internal ID22453972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:94690991..95007035hg38UCSC Ensembl
chr2:95356717..95672780hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38316045
hg19316064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868064
Supporting Variants
Samples
Known GenesANKRD20A8P, FAM95A, LOC442028, TEKT4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17396102
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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