A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500782



Internal ID22558719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120312347..120313763hg38UCSC Ensembl
chr7:119952401..119953817hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg381417
hg191417
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852853
Supporting Variants
Samples
Known GenesKCND2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500782
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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