A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488035



Internal ID22545952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74610443..74614551hg38UCSC Ensembl
chr2:74837570..74841678hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg384109
hg194109
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833718
Supporting Variants
Samples
Known GenesM1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488035
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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