A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392395



Internal ID22450265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113852816..113901287hg38UCSC Ensembl
chr3:113571663..113620134hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3848472
hg1948472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898677
Supporting Variants
Samples
Known GenesGRAMD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392395
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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