A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849243



Internal ID22624178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95342764..95353038hg38UCSC Ensembl
chr7:94972076..94982350hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3810275
hg1910275
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849243
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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