A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440263



Internal ID22498133
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 StatusS
Merged Variantsnsv5908161
Supporting Variants
Samples
Known GenesPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440263
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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