A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487636



Internal ID22545552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67960477..67964432hg38UCSC Ensembl
chr2:68187609..68191564hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383956
hg193956
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487636
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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