A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008985



Internal ID20576027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36205531..36206030hg38UCSC Ensembl
chr13:36779668..36780167hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487412
Supporting Variants
Samples
Known GenesCCDC169-SOHLH2, SOHLH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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