A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925976



Internal ID22701203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93233340..93233757hg38UCSC Ensembl
chr7:92862653..92863070hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437112
Samples
Known GenesCCDC132
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925976
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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