A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446486



Internal ID22504356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65106549..65795958hg38UCSC Ensembl
chr7:64566927..65260945hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38689410
hg19694019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920709
Supporting Variants
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446486
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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