A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441357



Internal ID22499227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77730801..77736962hg38UCSC Ensembl
chr6:78440518..78446679hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg386162
hg196162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891037
Supporting Variants
Samples
Known GenesMEI4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441357
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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