A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503704



Internal ID22561645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1805644..1806676hg38UCSC Ensembl
chr6:1805878..1806910hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381033
hg191033
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844494
Supporting Variants
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503704
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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