A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407573



Internal ID22465443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61481559..61481847hg38UCSC Ensembl
chr2:61708694..61708982hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886441
Supporting Variants
Samples
Known GenesXPO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407573
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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