A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908161



Internal ID22683371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137262562..137268423hg38UCSC Ensembl
chr7:136947309..136953170hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg385862
hg195862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440263
Samples
Known GenesPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908161
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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