A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144156



Internal ID21504666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75073566..75074149hg38UCSC Ensembl
chr7:74489402..74489985hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572534
Supporting Variants
SamplesNA19240
Known GenesWBSCR16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144156
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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