A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948625



Internal ID21368694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107770156..107770241hg38UCSC Ensembl
chr7:107410601..107410686hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198138
SamplesHG002
Known GenesSLC26A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948625
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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