A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997337



Internal ID65766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44188624..44189795hg38UCSC Ensembl
chr7:44228223..44229394hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489196
Supporting Variants
Samples
Known GenesGCK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997337
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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