A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082740



Internal ID20649780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:178529801..178680900hg38UCSC Ensembl
chr2:179394528..179545627hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38151100
hg19151100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347107
Supporting Variants
Samples
Known GenesMIR548N, TTN, TTN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0013


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