A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4388623



Internal ID21379758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97160090..97163548hg38UCSC Ensembl
chr7:96789402..96792860hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg383459
hg193459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704207
Samples
Known GenesACN9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4388623
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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