A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199556



Internal ID21338352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39150936..39151034hg38UCSC Ensembl
chr8:39008455..39008553hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946301
Supporting Variants
SamplesHG002
Known GenesADAM32
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199556
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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