A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488063



Internal ID22545980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77130270..77141484hg38UCSC Ensembl
chr2:77357396..77368610hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3811215
hg1911215
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834030
Supporting Variants
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488063
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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