A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507001



Internal ID22564949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43307793..43310107hg38UCSC Ensembl
chr7:43347392..43349706hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382315
hg192315
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846350
Supporting Variants
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507001
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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