A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506281



Internal ID22564227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35095675..35153575hg38UCSC Ensembl
chr7:35135287..35193187hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3857901
hg1957901
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846573
Supporting Variants
Samples
Known GenesDPY19L2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506281
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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