A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15198621



Internal ID21337417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84080545..84080871hg38UCSC Ensembl
chr7:83709861..83710187hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931394
Supporting Variants
SamplesHG002
Known GenesSEMA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15198621
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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