A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18003580



Internal ID20570620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75392487..75392988hg38UCSC Ensembl
chr12:75786267..75786768hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469637
Supporting Variants
Samples
Known GenesGLIPR1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18003580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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