A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490156



Internal ID267419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91079678..91104199hg38UCSC Ensembl
chr7:90708993..90733514hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3824522
hg1924522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999616
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490156
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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