A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504334



Internal ID22562277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2310663..2317965hg38UCSC Ensembl
chr6:2310897..2318199hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg387303
hg197303
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844569
Supporting Variants
Samples
Known GenesGMDS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504334
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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