A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971329



Internal ID22746264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35022695..35022695hg38UCSC Ensembl
chr19:35513599..35513599hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391044
Samples
Known GenesGRAMD1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971329
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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