A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431626



Internal ID22489496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155203527..155203588hg38UCSC Ensembl
chr7:154995237..154995298hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431626
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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