A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503382



Internal ID22561323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155001779..155003882hg38UCSC Ensembl
chr7:154793489..154795592hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg382104
hg192104
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861432
Supporting Variants
Samples
Known GenesPAXIP1, PAXIP1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503382
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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