A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177714



Internal ID20744754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72993730..73025316hg38UCSC Ensembl
chr10:74753488..74785074hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3831587
hg1931587
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449929
Supporting Variants
Samples
Known GenesP4HA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177714
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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