A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607086



Internal ID21799133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48915903..48916061hg38UCSC Ensembl
chr12:49309686..49309844hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032747
Supporting Variants
Samples
Known GenesCCDC65
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607086
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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