A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177534



Internal ID21316330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7870908..7870977hg38UCSC Ensembl
chr19:7935794..7935863hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931053
Supporting Variants
SamplesHG002
Known GenesFLJ22184
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177534
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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