A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505511



Internal ID22563455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32579743..32583178hg38UCSC Ensembl
chr7:32619355..32622790hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg383436
hg193436
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846930
Supporting Variants
Samples
Known GenesAVL9, DPY19L1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505511
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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