A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998330



Internal ID66429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72526779..72848779hg38UCSC Ensembl
chr7:71991764..72319359hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38322001
hg19327596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479835
Supporting Variants
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, TYW1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998330
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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