A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926109



Internal ID22701336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149485295..149492258hg38UCSC Ensembl
chr7:149182386..149189349hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386964
hg196964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439650
Samples
Known GenesZNF746
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926109
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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