A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002126



Internal ID69017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91857662..91893869hg38UCSC Ensembl
chr7:91486976..91523183hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3836208
hg1936208
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563019
Supporting Variants
Samples
Known GenesMTERF
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002126
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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