A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457601



Internal ID22515482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28544561..28556253hg38UCSC Ensembl
chr12:28697494..28709186hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3811693
hg1911693
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851630
Supporting Variants
Samples
Known GenesCCDC91
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457601
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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