A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449929



Internal ID21107482
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 StatusM
Merged Variants
Supporting Variantsnssv18177714
Samples
Known GenesP4HA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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