A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438998



Internal ID22496868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65103162..65765400hg38UCSC Ensembl
chr7:64563540..65230387hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38662239
hg19666848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922394
Supporting Variants
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438998
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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